# eHDSI Rare Disease - MyHealth@Eu MVC package v9.1.0

* [**Table of Contents**](toc.md)
* [**Artifacts Summary**](artifacts.md)
* **eHDSI Rare Disease**

## ValueSet: eHDSI Rare Disease 

| | |
| :--- | :--- |
| *Official URL*:http://terminology.ehdsi.eu/ValueSet/eHDSIRareDisease | *Version*:9.1.0 |
| Active as of 2026-05-08 | *Computable Name*:EHDSIRareDisease |
| *Other Identifiers:*OID:1.3.6.1.4.1.12559.11.10.1.3.1.42.63 | |
| **Copyright/Legal**: This Value Set includes a subset of the Orphanet Nomenclature Pack for codification which is released each year in July (https://www.orphadata.com/pack-nomenclature/). Countries that wish to translate the subset provided in this file should first check if an existing translation is available on Orphadata (either as part of the nomenclature pack or as one of the languages of the nomenclature alignment files) so as to not duplicate efforts. Translations into languages not already distributed by Orphanet should be validated by a medical doctor/committee to ensure their accuracy and the Orphanet Coordinating team should be notified (partnerships.orphanet@inserm.fr). Any modifications/updates a user wishes to make to an existing translation distributed by Orphanet should contact the Orphanet Coordinating Team (partnerships.orphanet@inserm.fr) | |

 
The Value Set is used to describe the problems and medication reasons. 

 **References** 

This value set is not used here; it may be used elsewhere (e.g. specifications and/or implementations that use this content)

### Logical Definition (CLD)

 

### Expansion

No Expansion for this valueset (Unknown Code System)

-------

 Explanation of the columns that may appear on this page: 

| | |
| :--- | :--- |
| Level | A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies |
| System | The source of the definition of the code (when the value set draws in codes defined elsewhere) |
| Code | The code (used as the code in the resource instance) |
| Display | The display (used in the*display*element of a[Coding](http://hl7.org/fhir/R4/datatypes.html#Coding)). If there is no display, implementers should not simply display the code, but map the concept into their application |
| Definition | An explanation of the meaning of the concept |
| Comments | Additional notes about how to use the code |



## Resource Content

```json
{
  "resourceType" : "ValueSet",
  "id" : "eHDSIRareDisease",
  "url" : "http://terminology.ehdsi.eu/ValueSet/eHDSIRareDisease",
  "identifier" : [{
    "system" : "urn:ietf:rfc:3986",
    "value" : "urn:oid:1.3.6.1.4.1.12559.11.10.1.3.1.42.63"
  }],
  "version" : "9.1.0",
  "name" : "EHDSIRareDisease",
  "title" : "eHDSI Rare Disease",
  "status" : "active",
  "experimental" : false,
  "date" : "2026-05-08T11:21:08+02:00",
  "publisher" : "MyHealth@Eu",
  "contact" : [{
    "name" : "MyHealth@Eu",
    "telecom" : [{
      "system" : "url",
      "value" : "https://health.ec.europa.eu/other-pages/basic-page/myhealtheu-flyer-addressed-patients-and-health-professionals_en"
    }]
  }],
  "description" : "The Value Set is used to describe the problems and medication reasons.",
  "copyright" : "This Value Set includes a subset of the Orphanet Nomenclature Pack for codification which is released each year in July (https://www.orphadata.com/pack-nomenclature/). Countries that wish to translate the subset provided in this file should first check if an existing translation is available on Orphadata (either as part of the nomenclature pack or as one of the languages of the nomenclature alignment files) so as to not duplicate efforts. Translations into languages not already distributed by Orphanet should be validated by a medical doctor/committee to ensure their accuracy and the Orphanet Coordinating team should be notified (partnerships.orphanet@inserm.fr). Any modifications/updates a user wishes to make to an existing translation distributed by Orphanet should contact the Orphanet Coordinating Team (partnerships.orphanet@inserm.fr)",
  "compose" : {
    "include" : [{
      "system" : "https://www.orpha.net",
      "concept" : [{
        "code" : "10",
        "display" : "48,XXYY syndrome"
      },
      {
        "code" : "100",
        "display" : "Ataxia-telangiectasia"
      },
      {
        "code" : "1000",
        "display" : "Ocular albinism with late-onset sensorineural deafness"
      },
      {
        "code" : "100000",
        "display" : "Reticular perineurioma"
      },
      {
        "code" : "100001",
        "display" : "Sclerosing perineurioma"
      },
      {
        "code" : "100002",
        "display" : "Extraneural perineurioma"
      },
      {
        "code" : "100003",
        "display" : "Intraneural perineurioma"
      },
      {
        "code" : "100006",
        "display" : "ABeta amyloidosis, Dutch type"
      },
      {
        "code" : "100008",
        "display" : "ACys amyloidosis"
      },
      {
        "code" : "100011",
        "display" : "Lissencephaly with cerebellar hypoplasia type A"
      },
      {
        "code" : "100012",
        "display" : "Lissencephaly with cerebellar hypoplasia type B"
      },
      {
        "code" : "100013",
        "display" : "Lissencephaly with cerebellar hypoplasia type C"
      },
      {
        "code" : "100014",
        "display" : "Lissencephaly with cerebellar hypoplasia type D"
      },
      {
        "code" : "100015",
        "display" : "Lissencephaly with cerebellar hypoplasia type E"
      },
      {
        "code" : "100016",
        "display" : "Lissencephaly with cerebellar hypoplasia type F"
      },
      {
        "code" : "100019",
        "display" : "Myelodysplastic neoplasm with increased blasts type 1"
      },
      {
        "code" : "100020",
        "display" : "Myelodysplastic neoplasm with increased blasts type 2"
      },
      {
        "code" : "100021",
        "display" : "Primary plasmacytoma of the bone"
      },
      {
        "code" : "100022",
        "display" : "Extramedullary soft tissue plasmacytoma"
      },
      {
        "code" : "100024",
        "display" : "Mu-heavy chain disease"
      },
      {
        "code" : "100025",
        "display" : "Alpha-heavy chain disease"
      },
      {
        "code" : "100026",
        "display" : "Gamma-heavy chain disease"
      },
      {
        "code" : "100031",
        "display" : "Hypoplastic amelogenesis imperfecta"
      },
      {
        "code" : "100032",
        "display" : "Hypocalcified amelogenesis imperfecta"
      },
      {
        "code" : "100033",
        "display" : "Hypomaturation amelogenesis imperfecta"
      },
      {
        "code" : "100034",
        "display" : "Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism"
      },
      {
        "code" : "100035",
        "display" : "Solitary necrotic nodule of the liver"
      },
      {
        "code" : "100043",
        "display" : "Autosomal dominant intermediate Charcot-Marie-Tooth disease type A"
      },
      {
        "code" : "100044",
        "display" : "Autosomal dominant intermediate Charcot-Marie-Tooth disease type B"
      },
      {
        "code" : "100045",
        "display" : "Autosomal dominant intermediate Charcot-Marie-Tooth disease type C"
      },
      {
        "code" : "100046",
        "display" : "Autosomal dominant intermediate Charcot-Marie-Tooth disease type D"
      },
      {
        "code" : "100047",
        "display" : "Isolated esophageal duplication cyst"
      },
      {
        "code" : "100048",
        "display" : "Isolated tubular duplication of the esophagus"
      },
      {
        "code" : "100050",
        "display" : "Hereditary angioedema type 1"
      },
      {
        "code" : "100051",
        "display" : "Hereditary angioedema type 2"
      },
      {
        "code" : "100054",
        "display" : "F12-related hereditary angioedema with normal C1Inh"
      },
      {
        "code" : "100055",
        "display" : "Acquired angioedema type 2"
      },
      {
        "code" : "100056",
        "display" : "Acquired angioedema type 1"
      },
      {
        "code" : "100057",
        "display" : "Renin-angiotensin-aldosterone system-blocker-induced angioedema"
      },
      {
        "code" : "100067",
        "display" : "Waterhouse-Friderichsen syndrome"
      },
      {
        "code" : "100069",
        "display" : "Semantic dementia"
      },
      {
        "code" : "100070",
        "display" : "Progressive non-fluent aphasia"
      },
      {
        "code" : "100071",
        "display" : "Mosaic trisomy 3 syndrome"
      },
      {
        "code" : "100073",
        "display" : "Neurogenic thoracic outlet syndrome"
      },
      {
        "code" : "100075",
        "display" : "Neuroendocrine tumor of stomach"
      },
      {
        "code" : "100078",
        "display" : "Ileal neuroendocrine tumor"
      },
      {
        "code" : "100079",
        "display" : "Neuroendocrine neoplasm of appendix"
      },
      {
        "code" : "100080",
        "display" : "Neuroendocrine tumor of the colon"
      },
      {
        "code" : "100081",
        "display" : "Neuroendocrine tumor of the rectum"
      },
      {
        "code" : "100082",
        "display" : "Neuroendocrine tumor of anal canal"
      },
      {
        "code" : "100083",
        "display" : "Laryngeal neuroendocrine tumor"
      },
      {
        "code" : "100084",
        "display" : "Middle ear neuroendocrine tumor"
      },
      {
        "code" : "100085",
        "display" : "Primary hepatic neuroendocrine carcinoma"
      },
      {
        "code" : "100086",
        "display" : "Gallbladder neuroendocrine tumor"
      },
      {
        "code" : "100093",
        "display" : "Carcinoid syndrome"
      },
      {
        "code" : "1001",
        "display" : "2q37 microdeletion syndrome"
      },
      {
        "code" : "1003",
        "display" : "Scalp defects-postaxial polydactyly syndrome"
      },
      {
        "code" : "1005",
        "display" : "Alopecia-contractures-dwarfism-intellectual disability syndrome"
      },
      {
        "code" : "1006",
        "display" : "Alopecia antibody deficiency"
      },
      {
        "code" : "1008",
        "display" : "Alopecia-epilepsy-pyorrhea-intellectual disability syndrome"
      },
      {
        "code" : "100924",
        "display" : "Porphyria due to ALA dehydratase deficiency"
      },
      {
        "code" : "100973",
        "display" : "FRAXE intellectual disability"
      },
      {
        "code" : "100974",
        "display" : "FRAXF syndrome"
      },
      {
        "code" : "100976",
        "display" : "Bathing suit ichthyosis"
      },
      {
        "code" : "100978",
        "display" : "Cloverleaf skull-asphyxiating thoracic dysplasia syndrome"
      },
      {
        "code" : "100984",
        "display" : "Autosomal dominant spastic paraplegia type 3"
      },
      {
        "code" : "100985",
        "display" : "Autosomal dominant spastic paraplegia type 4"
      },
      {
        "code" : "100986",
        "display" : "Autosomal recessive spastic paraplegia type 5A"
      },
      {
        "code" : "100988",
        "display" : "Autosomal dominant spastic paraplegia type 6"
      },
      {
        "code" : "100989",
        "display" : "Autosomal dominant spastic paraplegia type 8"
      },
      {
        "code" : "100991",
        "display" : "Autosomal dominant spastic paraplegia type 10"
      },
      {
        "code" : "100993",
        "display" : "Autosomal dominant spastic paraplegia type 12"
      },
      {
        "code" : "100994",
        "display" : "Autosomal dominant spastic paraplegia type 13"
      },
      {
        "code" : "100995",
        "display" : "Autosomal recessive spastic paraplegia type 14"
      },
      {
        "code" : "100996",
        "display" : "Autosomal recessive spastic paraplegia type 15"
      },
      {
        "code" : "100997",
        "display" : "X-linked spastic paraplegia type 16"
      },
      {
        "code" : "100998",
        "display" : "Autosomal dominant spastic paraplegia type 17"
      },
      {
        "code" : "100999",
        "display" : "Autosomal dominant spastic paraplegia type 19"
      },
      {
        "code" : "101",
        "display" : "Dentatorubral pallidoluysian atrophy"
      },
      {
        "code" : "1010",
        "display" : "Autosomal dominant palmoplantar keratoderma and congenital alopecia"
      },
      {
        "code" : "101000",
        "display" : "Autosomal recessive spastic paraplegia type 20"
      },
      {
        "code" : "101001",
        "display" : "Autosomal recessive spastic paraplegia type 21"
      },
      {
        "code" : "101003",
        "display" : "Autosomal recessive spastic paraplegia type 23"
      },
      {
        "code" : "101004",
        "display" : "Autosomal recessive spastic paraplegia type 24"
      },
      {
        "code" : "101005",
        "display" : "Autosomal recessive spastic paraplegia type 25"
      },
      {
        "code" : "101006",
        "display" : "Autosomal recessive spastic paraplegia type 26"
      },
      {
        "code" : "101007",
        "display" : "Autosomal recessive spastic paraplegia type 27"
      },
      {
        "code" : "101008",
        "display" : "Autosomal recessive spastic paraplegia type 28"
      },
      {
        "code" : "101009",
        "display" : "Autosomal dominant spastic paraplegia type 29"
      },
      {
        "code" : "101010",
        "display" : "Autosomal spastic paraplegia type 30"
      },
      {
        "code" : "101011",
        "display" : "Autosomal dominant spastic paraplegia type 31"
      },
      {
        "code" : "101016",
        "display" : "Romano-Ward syndrome"
      },
      {
        "code" : "101023",
        "display" : "Cleft hard palate"
      },
      {
        "code" : "101028",
        "display" : "Transaldolase deficiency"
      },
      {
        "code" : "101029",
        "display" : "Sub-cortical nodular heterotopia"
      },
      {
        "code" : "101030",
        "display" : "Subependymal nodular heterotopia"
      },
      {
        "code" : "101039",
        "display" : "Female restricted epilepsy with intellectual disability"
      },
      {
        "code" : "101041",
        "display" : "Familial hypofibrinogenemia"
      },
      {
        "code" : "101043",
        "display" : "Congenital aortic valve dysplasia"
      },
      {
        "code" : "101046",
        "display" : "Epilepsy with auditory features"
      },
      {
        "code" : "101049",
        "display" : "Familial hypocalciuric hypercalcemia type 2"
      },
      {
        "code" : "101050",
        "display" : "Familial hypocalciuric hypercalcemia type 3"
      },
      {
        "code" : "101063",
        "display" : "Situs inversus totalis"
      },
      {
        "code" : "101068",
        "display" : "Congenital stromal corneal dystrophy"
      },
      {
        "code" : "101070",
        "display" : "Bilateral frontoparietal polymicrogyria"
      },
      {
        "code" : "101071",
        "display" : "Unilateral hemispheric polymicrogyria"
      },
      {
        "code" : "101075",
        "display" : "X-linked Charcot-Marie-Tooth disease type 1"
      },
      {
        "code" : "101076",
        "display" : "X-linked Charcot-Marie-Tooth disease type 2"
      },
      {
        "code" : "101077",
        "display" : "X-linked Charcot-Marie-Tooth disease type 3"
      },
      {
        "code" : "101078",
        "display" : "X-linked Charcot-Marie-Tooth disease type 4"
      },
      {
        "code" : "101081",
        "display" : "Charcot-Marie-Tooth disease type 1A"
      },
      {
        "code" : "101082",
        "display" : "Charcot-Marie-Tooth disease type 1B"
      },
      {
        "code" : "101083",
        "display" : "Charcot-Marie-Tooth disease type 1C"
      },
      {
        "code" : "101084",
        "display" : "Charcot-Marie-Tooth disease type 1D"
      },
      {
        "code" : "101085",
        "display" : "Charcot-Marie-Tooth disease type 1F"
      },
      {
        "code" : "101088",
        "display" : "X-linked hyper-IgM syndrome"
      },
      {
        "code" : "101089",
        "display" : "Hyper-IgM syndrome type 2"
      },
      {
        "code" : "101090",
        "display" : "Hyper-IgM syndrome type 3"
      },
      {
        "code" : "101091",
        "display" : "Hyper-IgM syndrome type 4"
      },
      {
        "code" : "101092",
        "display" : "Hyper-IgM syndrome type 5"
      },
      {
        "code" : "101097",
        "display" : "Autosomal recessive Charcot-Marie-Tooth disease with hoarseness"
      },
      {
        "code" : "101101",
        "display" : "Charcot-Marie-Tooth disease type 2B2"
      },
      {
        "code" : "101102",
        "display" : "Charcot-Marie-Tooth disease type 2H"
      },
      {
        "code" : "101104",
        "display" : "Marin-Amat syndrome"
      },
      {
        "code" : "101108",
        "display" : "Spinocerebellar ataxia type 23"
      },
      {
        "code" : "101109",
        "display" : "Spinocerebellar ataxia type 28"
      },
      {
        "code" : "101110",
        "display" : "Spinocerebellar ataxia type 20"
      },
      {
        "code" : "101111",
        "display" : "Spinocerebellar ataxia type 25"
      },
      {
        "code" : "101112",
        "display" : "Spinocerebellar ataxia type 26"
      },
      {
        "code" : "101150",
        "display" : "Autosomal recessive dopa-responsive dystonia"
      },
      {
        "code" : "101206",
        "display" : "Pulmonary valve agenesis-tetralogy of Fallot-absence of ductus arteriosus syndrome"
      },
      {
        "code" : "101330",
        "display" : "Porphyria cutanea tarda"
      },
      {
        "code" : "101334",
        "display" : "African tick typhus"
      },
      {
        "code" : "101351",
        "display" : "Familial isolated congenital asplenia"
      },
      {
        "code" : "1014",
        "display" : "Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome"
      },
      {
        "code" : "101685",
        "display" : "Rare non-syndromic intellectual disability"
      },
      {
        "code" : "1018",
        "display" : "X-linked Alport syndrome-diffuse leiomyomatosis"
      },
      {
        "code" : "101932",
        "display" : "Anomaly of the mitral subvalvular apparatus"
      },
      {
        "code" : "102",
        "display" : "Multiple system atrophy"
      },
      {
        "code" : "1020",
        "display" : "Early-onset autosomal dominant Alzheimer disease"
      },
      {
        "code" : "1021",
        "display" : "Amaurosis-hypertrichosis syndrome"
      },
      {
        "code" : "1023",
        "display" : "Congenital generalized hypertrichosis, Ambras type"
      },
      {
        "code" : "102379",
        "display" : "Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent"
      },
      {
        "code" : "102381",
        "display" : "Acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor"
      },
      {
        "code" : "102724",
        "display" : "Acute myeloid leukemia with t(8;21)(q22;q22) translocation"
      },
      {
        "code" : "1028",
        "display" : "Amelo-onycho-hypohidrotic syndrome"
      },
      {
        "code" : "1031",
        "display" : "Enamel-renal syndrome"
      },
      {
        "code" : "1035",
        "display" : "Beta-mercaptolactate cysteine disulfiduria"
      },
      {
        "code" : "103907",
        "display" : "Chronic diarrhea due to glucoamylase deficiency"
      },
      {
        "code" : "103908",
        "display" : "Congenital sodium diarrhea"
      },
      {
        "code" : "103909",
        "display" : "Trehalase deficiency"
      },
      {
        "code" : "103910",
        "display" : "Congenital enterocyte heparan sulfate deficiency"
      },
      {
        "code" : "103918",
        "display" : "Tropical pancreatitis"
      },
      {
        "code" : "103920",
        "display" : "Undetermined colitis"
      },
      {
        "code" : "104",
        "display" : "Leber hereditary optic neuropathy"
      },
      {
        "code" : "1040",
        "display" : "Metaphyseal anadysplasia"
      },
      {
        "code" : "104075",
        "display" : "Adenocarcinoma of the small intestine"
      },
      {
        "code" : "104076",
        "display" : "Leiomyosarcoma of small intestine"
      },
      {
        "code" : "104077",
        "display" : "Myopathic intestinal pseudoobstruction"
      },
      {
        "code" : "104078",
        "display" : "Unclassified intestinal pseudoobstruction"
      },
      {
        "code" : "1041",
        "display" : "Hydrops fetalis"
      },
      {
        "code" : "1046",
        "display" : "Lethal hemolytic anemia-genital anomalies syndrome"
      },
      {
        "code" : "1048",
        "display" : "Isolated anencephaly/exencephaly"
      },
      {
        "code" : "105",
        "display" : "Atresia of urethra"
      },
      {
        "code" : "1051",
        "display" : "Ramos-Arroyo syndrome"
      },
      {
        "code" : "1052",
        "display" : "Mosaic variegated aneuploidy syndrome"
      },
      {
        "code" : "1053",
        "display" : "Vein of Galen aneurysmal malformation"
      },
      {
        "code" : "1054",
        "display" : "Aneurysm of sinus of Valsalva"
      },
      {
        "code" : "1055",
        "display" : "Congenital left ventricular aneurysm"
      },
      {
        "code" : "1059",
        "display" : "Blue rubber bleb nevus"
      },
      {
        "code" : "1062",
        "display" : "Hereditary neurocutaneous malformation"
      },
      {
        "code" : "1063",
        "display" : "Tufted angioma"
      },
      {
        "code" : "1064",
        "display" : "Aniridia-renal agenesis-psychomotor retardation syndrome"
      },
      {
        "code" : "1065",
        "display" : "Aniridia-cerebellar ataxia-intellectual disability syndrome"
      },
      {
        "code" : "1067",
        "display" : "Aniridia-ptosis-intellectual disability-familial obesity syndrome"
      },
      {
        "code" : "1068",
        "display" : "Aniridia-intellectual disability syndrome"
      },
      {
        "code" : "1069",
        "display" : "Aniridia-absent patella syndrome"
      },
      {
        "code" : "107",
        "display" : "BOR syndrome"
      },
      {
        "code" : "1070",
        "display" : "Anisakiasis"
      },
      {
        "code" : "1071",
        "display" : "Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome"
      },
      {
        "code" : "1072",
        "display" : "Ankyloblepharon filiforme adnatum-cleft palate syndrome"
      },
      {
        "code" : "1074",
        "display" : "Ankyloblepharon filiforme adnatum-imperforate anus syndrome"
      },
      {
        "code" : "1077",
        "display" : "Dental ankylosis"
      },
      {
        "code" : "1078",
        "display" : "Thumb stiffness-brachydactyly-intellectual disability syndrome"
      },
      {
        "code" : "108",
        "display" : "Babesiosis"
      },
      {
        "code" : "1083",
        "display" : "Microlissencephaly"
      },
      {
        "code" : "1084",
        "display" : "Isolated lissencephaly type 1 without known genetic defects"
      },
      {
        "code" : "109",
        "display" : "Bannayan-Riley-Ruvalcaba syndrome"
      },
      {
        "code" : "1094",
        "display" : "Anonychia-microcephaly syndrome"
      },
      {
        "code" : "11",
        "display" : "Pentasomy X syndrome"
      },
      {
        "code" : "110",
        "display" : "Bardet-Biedl syndrome"
      },
      {
        "code" : "1101",
        "display" : "Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome"
      },
      {
        "code" : "1104",
        "display" : "Anophthalmia plus syndrome"
      },
      {
        "code" : "1106",
        "display" : "Microphthalmia with limb anomalies"
      },
      {
        "code" : "111",
        "display" : "Barth syndrome"
      },
      {
        "code" : "1110",
        "display" : "Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome"
      },
      {
        "code" : "1112",
        "display" : "Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome"
      },
      {
        "code" : "1113",
        "display" : "Aphalangy-syndactyly-microcephaly syndrome"
      },
      {
        "code" : "1114",
        "display" : "Aplasia cutis congenita"
      },
      {
        "code" : "1116",
        "display" : "Aplasia cutis congenita-intestinal lymphangiectasia syndrome"
      },
      {
        "code" : "1117",
        "display" : "Aplasia cutis-myopia syndrome"
      },
      {
        "code" : "1118",
        "display" : "Fibular aplasia-ectrodactyly syndrome"
      },
      {
        "code" : "112",
        "display" : "Bartter syndrome"
      },
      {
        "code" : "1120",
        "display" : "Lung agenesis-heart defect-thumb anomalies syndrome"
      },
      {
        "code" : "1121",
        "display" : "Radial deficiency-tibial hypoplasia syndrome"
      },
      {
        "code" : "1122",
        "display" : "Ulnar hypoplasia-split foot syndrome"
      },
      {
        "code" : "1123",
        "display" : "Caudal appendage-deafness syndrome"
      },
      {
        "code" : "1125",
        "display" : "Ocular motor apraxia, Cogan type"
      },
      {
        "code" : "1126",
        "display" : "Aprosencephaly cerebellar dysgenesis"
      },
      {
        "code" : "1129",
        "display" : "Arachnodactyly-abnormal ossification-intellectual disability syndrome"
      },
      {
        "code" : "113",
        "display" : "Bazex-Dupré-Christol syndrome"
      },
      {
        "code" : "1130",
        "display" : "Arachnodactyly-intellectual disability-dysmorphism syndrome"
      },
      {
        "code" : "1131",
        "display" : "X-linked mandibulofacial dysostosis"
      },
      {
        "code" : "1133",
        "display" : "AREDYLD syndrome"
      },
      {
        "code" : "1134",
        "display" : "Isolated arrhinia"
      },
      {
        "code" : "114",
        "display" : "Auriculoosteodysplasia"
      },
      {
        "code" : "1143",
        "display" : "Neurogenic arthrogryposis multiplex congenita"
      },
      {
        "code" : "1144",
        "display" : "Arthrogryposis-like hand anomaly-sensorineural deafness syndrome"
      },
      {
        "code" : "1145",
        "display" : "Infantile-onset X-linked spinal muscular atrophy"
      },
      {
        "code" : "1146",
        "display" : "Distal arthrogryposis type 1"
      },
      {
        "code" : "1147",
        "display" : "Sheldon-Hall syndrome"
      },
      {
        "code" : "1149",
        "display" : "Kuskokwim syndrome"
      },
      {
        "code" : "115",
        "display" : "Congenital contractural arachnodactyly"
      },
      {
        "code" : "1150",
        "display" : "Arthrogryposis multiplex congenita-whistling face syndrome"
      },
      {
        "code" : "1154",
        "display" : "Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome"
      },
      {
        "code" : "1159",
        "display" : "Progressive pseudorheumatoid dysplasia"
      },
      {
        "code" : "116",
        "display" : "Beckwith-Wiedemann syndrome"
      },
      {
        "code" : "1160",
        "display" : "Chylous ascites"
      },
      {
        "code" : "1163",
        "display" : "Aspergillosis"
      },
      {
        "code" : "1164",
        "display" : "Allergic bronchopulmonary aspergillosis"
      },
      {
        "code" : "1166",
        "display" : "Congenital unilateral hypoplasia of depressor anguli oris"
      },
      {
        "code" : "1168",
        "display" : "Ataxia-oculomotor apraxia type 1"
      },
      {
        "code" : "117",
        "display" : "Behçet disease"
      },
      {
        "code" : "1170",
        "display" : "Autosomal recessive cerebelloparenchymal disorder type 3"
      },
      {
        "code" : "1171",
        "display" : "Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome"
      },
      {
        "code" : "1173",
        "display" : "Cerebellar ataxia-hypogonadism syndrome"
      },
      {
        "code" : "1174",
        "display" : "Cerebellar ataxia-ectodermal dysplasia syndrome"
      },
      {
        "code" : "1175",
        "display" : "X-linked progressive cerebellar ataxia"
      },
      {
        "code" : "1177",
        "display" : "Early-onset cerebellar ataxia with retained tendon reflexes"
      },
      {
        "code" : "1178",
        "display" : "Ataxia-tapetoretinal degeneration syndrome"
      },
      {
        "code" : "1179",
        "display" : "Benign paroxysmal tonic upgaze of childhood with ataxia"
      },
      {
        "code" : "118",
        "display" : "Beta-mannosidosis"
      },
      {
        "code" : "1180",
        "display" : "Ataxia-hypogonadism-choroidal dystrophy syndrome"
      },
      {
        "code" : "1182",
        "display" : "Spastic ataxia with congenital miosis"
      },
      {
        "code" : "1183",
        "display" : "Opsoclonus-myoclonus syndrome"
      },
      {
        "code" : "1184",
        "display" : "Ataxia-photosensitivity-short stature syndrome"
      },
      {
        "code" : "1185",
        "display" : "Spinocerebellar ataxia-dysmorphism syndrome"
      },
      {
        "code" : "1186",
        "display" : "Infantile-onset spinocerebellar ataxia"
      },
      {
        "code" : "1187",
        "display" : "Lethal ataxia with deafness and optic atrophy"
      },
      {
        "code" : "1188",
        "display" : "Ataxia-deafness-intellectual disability syndrome"
      },
      {
        "code" : "119",
        "display" : "Beta-sarcoglycan-related limb-girdle muscular dystrophy R4"
      },
      {
        "code" : "1190",
        "display" : "Atelosteogenesis type I"
      },
      {
        "code" : "1192",
        "display" : "Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome"
      },
      {
        "code" : "1193",
        "display" : "Atkin-Flaitz syndrome"
      },
      {
        "code" : "1194",
        "display" : "TMEM70-related mitochondrial encephalo-cardio-myopathy"
      },
      {
        "code" : "1195",
        "display" : "Congenital atransferrinemia"
      },
      {
        "code" : "1198",
        "display" : "Colonic atresia"
      },
      {
        "code" : "1199",
        "display" : "Esophageal atresia"
      },
      {
        "code" : "1200",
        "display" : "Burn-McKeown syndrome"
      },
      {
        "code" : "1201",
        "display" : "Small bowel atresia"
      },
      {
        "code" : "1202",
        "display" : "Larynx atresia"
      },
      {
        "code" : "1203",
        "display" : "Duodenal atresia"
      },
      {
        "code" : "1205",
        "display" : "Mitral atresia"
      },
      {
        "code" : "1207",
        "display" : "Pulmonary atresia with ventricular septal defect"
      },
      {
        "code" : "1208",
        "display" : "Pulmonary atresia-intact ventricular septum syndrome"
      },
      {
        "code" : "1209",
        "display" : "Tricuspid atresia"
      },
      {
        "code" : "1214",
        "display" : "Progressive hemifacial atrophy"
      },
      {
        "code" : "1215",
        "display" : "Autosomal dominant optic atrophy plus syndrome"
      },
      {
        "code" : "1216",
        "display" : "Autosomal dominant congenital benign spinal muscular atrophy"
      },
      {
        "code" : "1217",
        "display" : "Spinal atrophy-ophthalmoplegia-pyramidal syndrome"
      },
      {
        "code" : "122",
        "display" : "Birt-Hogg-Dubé syndrome"
      },
      {
        "code" : "1221",
        "display" : "Cheilitis glandularis"
      },
      {
        "code" : "1223",
        "display" : "Balantidiasis"
      },
      {
        "code" : "1225",
        "display" : "Baller-Gerold syndrome"
      },
      {
        "code" : "1226",
        "display" : "Bamforth-Lazarus syndrome"
      },
      {
        "code" : "1227",
        "display" : "Bangstad syndrome"
      },
      {
        "code" : "1228",
        "display" : "Banki syndrome"
      },
      {
        "code" : "1229",
        "display" : "Congenital intrauterine infection-like syndrome"
      },
      {
        "code" : "123",
        "display" : "Björnstad syndrome"
      },
      {
        "code" : "1231",
        "display" : "Barber-Say syndrome"
      },
      {
        "code" : "1234",
        "display" : "Bartsocas-Papas syndrome"
      },
      {
        "code" : "1236",
        "display" : "Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome"
      },
      {
        "code" : "1237",
        "display" : "Beemer-Ertbruggen syndrome"
      },
      {
        "code" : "1239",
        "display" : "Behr syndrome"
      },
      {
        "code" : "124",
        "display" : "Diamond-Blackfan anemia"
      },
      {
        "code" : "1241",
        "display" : "Bencze syndrome"
      },
      {
        "code" : "1243",
        "display" : "Best vitelliform macular dystrophy"
      },
      {
        "code" : "1246",
        "display" : "Brachydactyly-nystagmus-cerebellar ataxia syndrome"
      },
      {
        "code" : "1247",
        "display" : "Schistosomiasis"
      },
      {
        "code" : "1248",
        "display" : "Maxillonasal dysplasia"
      },
      {
        "code" : "125",
        "display" : "Bloom syndrome"
      },
      {
        "code" : "1252",
        "display" : "Blepharonasofacial malformation syndrome"
      },
      {
        "code" : "1253",
        "display" : "Ascher syndrome"
      },
      {
        "code" : "1259",
        "display" : "Blepharoptosis-myopia-ectopia lentis syndrome"
      },
      {
        "code" : "126",
        "display" : "Blepharophimosis-ptosis-epicanthus inversus syndrome"
      },
      {
        "code" : "1261",
        "display" : "Bonnemann-Meinecke-Reich syndrome"
      },
      {
        "code" : "1262",
        "display" : "Böök syndrome"
      },
      {
        "code" : "1263",
        "display" : "Boomerang dysplasia"
      },
      {
        "code" : "1264",
        "display" : "Tricho-retino-dento-digital syndrome"
      },
      {
        "code" : "1267",
        "display" : "Botulism"
      },
      {
        "code" : "127",
        "display" : "Borjeson-Forssman-Lehmann syndrome"
      },
      {
        "code" : "1270",
        "display" : "Bowen-Conradi syndrome"
      },
      {
        "code" : "1272",
        "display" : "Aymé-Gripp syndrome"
      },
      {
        "code" : "1275",
        "display" : "Brachydactyly-elbow wrist dysplasia syndrome"
      },
      {
        "code" : "1276",
        "display" : "Brachydactyly-arterial hypertension syndrome"
      },
      {
        "code" : "1277",
        "display" : "Brachydactyly-mesomelia-intellectual disability-heart defects syndrome"
      },
      {
        "code" : "1278",
        "display" : "Brachydactyly-preaxial hallux varus syndrome"
      },
      {
        "code" : "128",
        "display" : "Diphyllobothriasis"
      },
      {
        "code" : "129",
        "display" : "Pseudopelade of Brocq"
      },
      {
        "code" : "1292",
        "display" : "Brachymorphism-onychodysplasia-dysphalangism syndrome"
      },
      {
        "code" : "1295",
        "display" : "Brachytelephalangy-dysmorphism-Kallmann syndrome"
      },
      {
        "code" : "1296",
        "display" : "Lambert syndrome"
      },
      {
        "code" : "1297",
        "display" : "Branchio-oculo-facial syndrome"
      },
      {
        "code" : "1299",
        "display" : "Branchioskeletogenital syndrome"
      },
      {
        "code" : "13",
        "display" : "6-pyruvoyl-tetrahydropterin synthase deficiency"
      },
      {
        "code" : "130",
        "display" : "Brugada syndrome"
      },
      {
        "code" : "1300",
        "display" : "Autosomal dominant popliteal pterygium syndrome"
      },
      {
        "code" : "1302",
        "display" : "Cryptogenic organizing pneumonia"
      },
      {
        "code" : "1304",
        "display" : "Brucellosis"
      },
      {
        "code" : "1305",
        "display" : "Feingold syndrome"
      },
      {
        "code" : "1307",
        "display" : "Distal limb deficiencies-micrognathia syndrome"
      },
      {
        "code" : "1308",
        "display" : "C syndrome"
      },
      {
        "code" : "1309",
        "display" : "Medullary sponge kidney"
      },
      {
        "code" : "131",
        "display" : "Budd-Chiari syndrome"
      },
      {
        "code" : "1310",
        "display" : "Caffey disease"
      },
      {
        "code" : "1313",
        "display" : "Infantile choroidocerebral calcification syndrome"
      },
      {
        "code" : "1314",
        "display" : "Symmetrical thalamic calcifications"
      },
      {
        "code" : "1318",
        "display" : "Campomelia, Cumming type"
      },
      {
        "code" : "1319",
        "display" : "Camptobrachydactyly"
      },
      {
        "code" : "132",
        "display" : "Hereditary butyrylcholinesterase deficiency"
      },
      {
        "code" : "1320",
        "display" : "Idiopathic camptocormia"
      },
      {
        "code" : "1321",
        "display" : "Camptodactyly-fibrous tissue hyperplasia-skeletal anomalies syndrome"
      },
      {
        "code" : "1323",
        "display" : "Camptodactyly-joint contractures-facial skeletal defects syndrome"
      },
      {
        "code" : "1325",
        "display" : "Camptodactyly-taurinuria syndrome"
      },
      {
        "code" : "1326",
        "display" : "Camptodactyly syndrome, Guadalajara type 2"
      },
      {
        "code" : "1327",
        "display" : "Camptodactyly syndrome, Guadalajara type 1"
      },
      {
        "code" : "1328",
        "display" : "Camurati-Engelmann disease"
      },
      {
        "code" : "1329",
        "display" : "Complete atrioventricular septal defect"
      },
      {
        "code" : "133",
        "display" : "Chronic beryllium disease"
      },
      {
        "code" : "1330",
        "display" : "Partial atrioventricular septal defect"
      },
      {
        "code" : "1331",
        "display" : "Familial prostate cancer"
      },
      {
        "code" : "1332",
        "display" : "Medullary thyroid carcinoma"
      },
      {
        "code" : "1333",
        "display" : "Familial pancreatic carcinoma"
      },
      {
        "code" : "1334",
        "display" : "Chronic mucocutaneous candidiasis"
      },
      {
        "code" : "1335",
        "display" : "Pentalogy of Cantrell"
      },
      {
        "code" : "1336",
        "display" : "Hyperkeratosis-hyperpigmentation syndrome"
      },
      {
        "code" : "1338",
        "display" : "Heart defect-tongue hamartoma-polysyndactyly syndrome"
      },
      {
        "code" : "134",
        "display" : "Beta-ketothiolase deficiency"
      },
      {
        "code" : "1340",
        "display" : "Cardiofaciocutaneous syndrome"
      },
      {
        "code" : "1342",
        "display" : "Heart-hand syndrome type 3"
      },
      {
        "code" : "1344",
        "display" : "Isolated atrial standstill"
      },
      {
        "code" : "1345",
        "display" : "Cardiomyopathy-cataract-hip spine disease syndrome"
      },
      {
        "code" : "1349",
        "display" : "Mitochondrial DNA-related cardiomyopathy and hearing loss"
      },
      {
        "code" : "135",
        "display" : "CACH syndrome"
      },
      {
        "code" : "1350",
        "display" : "Heart-hand syndrome type 2"
      },
      {
        "code" : "1352",
        "display" : "Atrioventricular defect-blepharophimosis-radial and anal defect syndrome"
      },
      {
        "code" : "1354",
        "display" : "Heart defects-limb shortening syndrome"
      },
      {
        "code" : "1355",
        "display" : "Congenital heart defect-round face-developmental delay syndrome"
      },
      {
        "code" : "1358",
        "display" : "Carey-Fineman-Ziter syndrome"
      },
      {
        "code" : "1359",
        "display" : "Carney complex"
      },
      {
        "code" : "136",
        "display" : "Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy"
      },
      {
        "code" : "1361",
        "display" : "Carnosinase deficiency"
      },
      {
        "code" : "1366",
        "display" : "Autosomal recessive palmoplantar keratoderma and congenital alopecia"
      },
      {
        "code" : "1368",
        "display" : "Cataract-ataxia-deafness syndrome"
      },
      {
        "code" : "1369",
        "display" : "Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome"
      },
      {
        "code" : "1373",
        "display" : "Cataract-aberrant oral frenula-growth delay syndrome"
      },
      {
        "code" : "1375",
        "display" : "Cataract-hypertrichosis-intellectual disability syndrome"
      },
      {
        "code" : "137577",
        "display" : "Neonatal hypoxic and ischemic brain injury"
      },
      {
        "code" : "137583",
        "display" : "Vulvar intraepithelial neoplasia"
      },
      {
        "code" : "137593",
        "display" : "Infectious epithelial keratitis"
      },
      {
        "code" : "137596",
        "display" : "Neurotrophic keratopathy"
      },
      {
        "code" : "137599",
        "display" : "Herpes simplex virus stromal keratitis"
      },
      {
        "code" : "137602",
        "display" : "Corneal endotheliitis"
      },
      {
        "code" : "137605",
        "display" : "Legius syndrome"
      },
      {
        "code" : "137608",
        "display" : "Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome"
      },
      {
        "code" : "137617",
        "display" : "Nephrogenic systemic fibrosis"
      },
      {
        "code" : "137622",
        "display" : "Intractable diarrhea-choanal atresia-eye anomalies syndrome"
      },
      {
        "code" : "137625",
        "display" : "Glycogen storage disease due to muscle and heart glycogen synthase deficiency"
      },
      {
        "code" : "137628",
        "display" : "Cardiac anomalies-heterotaxy syndrome"
      },
      {
        "code" : "137631",
        "display" : "Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome"
      },
      {
        "code" : "137634",
        "display" : "Overgrowth-macrocephaly-facial dysmorphism syndrome"
      },
      {
        "code" : "137639",
        "display" : "Hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome"
      },
      {
        "code" : "137672",
        "display" : "Pellucid marginal degeneration"
      },
      {
        "code" : "137675",
        "display" : "Histiocytoid cardiomyopathy"
      },
      {
        "code" : "137678",
        "display" : "Spondyloepiphyseal dysplasia with metatarsal shortening"
      },
      {
        "code" : "137681",
        "display" : "Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1"
      },
      {
        "code" : "137686",
        "display" : "Asherman syndrome"
      },
      {
        "code" : "137698",
        "display" : "Cytomegalovirus disease in patients with impaired cell mediated immunity deemed at risk"
      },
      {
        "code" : "1377",
        "display" : "Cataract-microcornea syndrome"
      },
      {
        "code" : "137754",
        "display" : "Aminoacylase 1 deficiency"
      },
      {
        "code" : "137776",
        "display" : "Lethal congenital contracture syndrome type 2"
      },
      {
        "code" : "137783",
        "display" : "Lethal congenital contracture syndrome type 3"
      },
      {
        "code" : "137810",
        "display" : "Nodular cutaneous amyloidosis"
      },
      {
        "code" : "137814",
        "display" : "Macular amyloidosis"
      },
      {
        "code" : "137817",
        "display" : "Arachnoiditis"
      },
      {
        "code" : "137820",
        "display" : "Extrapelvic endometriosis"
      },
      {
        "code" : "137831",
        "display" : "X-linked intellectual disability-cerebellar hypoplasia syndrome"
      },
      {
        "code" : "137834",
        "display" : "Frank-Ter Haar syndrome"
      },
      {
        "code" : "137839",
        "display" : "Lemierre syndrome"
      },
      {
        "code" : "137867",
        "display" : "Madras motor neuron disease"
      },
      {
        "code" : "137888",
        "display" : "Auriculocondylar syndrome"
      },
      {
        "code" : "137893",
        "display" : "Male infertility due to large-headed multiflagellar polyploid spermatozoa"
      },
      {
        "code" : "137898",
        "display" : "Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome"
      },
      {
        "code" : "137908",
        "display" : "Hypotonia with lactic acidemia and hyperammonemia"
      },
      {
        "code" : "137914",
        "display" : "Choanal atresia"
      },
      {
        "code" : "137917",
        "display" : "Choanal atresia, unilateral"
      },
      {
        "code" : "137920",
        "display" : "Choanal atresia, bilateral"
      },
      {
        "code" : "137926",
        "display" : "Primary laryngeal lymphangioma"
      },
      {
        "code" : "137929",
        "display" : "Neonatal brainstem dysfunction"
      },
      {
        "code" : "137932",
        "display" : "Congenital laryngeal palsy"
      },
      {
        "code" : "137935",
        "display" : "Airway infantile hemangioma"
      },
      {
        "code" : "138",
        "display" : "CHARGE syndrome"
      },
      {
        "code" : "1380",
        "display" : "Cataract-nephropathy-encephalopathy syndrome"
      },
      {
        "code" : "1381",
        "display" : "Cataract-intellectual disability-anal atresia-urinary defects syndrome"
      },
      {
        "code" : "1383",
        "display" : "Cataract-deafness-hypogonadism syndrome"
      },
      {
        "code" : "1387",
        "display" : "Cataract-intellectual disability-hypogonadism syndrome"
      },
      {
        "code" : "1388",
        "display" : "Catel-Manzke syndrome"
      },
      {
        "code" : "1389",
        "display" : "Cortical blindness-intellectual disability-polydactyly syndrome"
      },
      {
        "code" : "139",
        "display" : "CHILD syndrome"
      },
      {
        "code" : "1390",
        "display" : "Night blindness-skeletal anomalies-dysmorphism syndrome"
      },
      {
        "code" : "1393",
        "display" : "Cerebrocostomandibular syndrome"
      },
      {
        "code" : "139396",
        "display" : "X-linked cerebral adrenoleukodystrophy"
      },
      {
        "code" : "139399",
        "display" : "Adrenomyeloneuropathy"
      },
      {
        "code" : "1394",
        "display" : "Cerebrofaciothoracic dysplasia"
      },
      {
        "code" : "139402",
        "display" : "Drug reaction with eosinophilia and systemic symptoms"
      },
      {
        "code" : "139406",
        "display" : "Encephalopathy due to prosaposin deficiency"
      },
      {
        "code" : "139411",
        "display" : "Carney triad"
      },
      {
        "code" : "139414",
        "display" : "Congenital panfollicular nevus"
      },
      {
        "code" : "139417",
        "display" : "Acute transverse myelitis"
      },
      {
        "code" : "139423",
        "display" : "Idiopathic acute transverse myelitis"
      },
      {
        "code" : "139426",
        "display" : "Perioral myoclonia with absences"
      },
      {
        "code" : "139431",
        "display" : "Epilepsy with eyelid myoclonia"
      },
      {
        "code" : "139436",
        "display" : "Multicentric reticulohistiocytosis"
      },
      {
        "code" : "139441",
        "display" : "Hypomyelination with atrophy of basal ganglia and cerebellum"
      },
      {
        "code" : "139444",
        "display" : "Leukoencephalopathy with bilateral anterior temporal lobe cysts"
      },
      {
        "code" : "139447",
        "display" : "Progressive cavitating leukoencephalopathy"
      },
      {
        "code" : "139450",
        "display" : "Microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome"
      },
      {
        "code" : "139455",
        "display" : "Autosomal recessive bestrophinopathy"
      },
      {
        "code" : "139466",
        "display" : "SERKAL syndrome"
      },
      {
        "code" : "139471",
        "display" : "Microphthalmia with brain and digit anomalies"
      },
      {
        "code" : "139474",
        "display" : "17q11.2 microduplication syndrome"
      },
      {
        "code" : "139480",
        "display" : "Autosomal recessive spastic paraplegia type 39"
      },
      {
        "code" : "139485",
        "display" : "Autosomal recessive ataxia due to ubiquinone deficiency"
      },
      {
        "code" : "139507",
        "display" : "Dietary iron overload disease"
      },
      {
        "code" : "139512",
        "display" : "Neuropathy with hearing impairment"
      },
      {
        "code" : "139515",
        "display" : "Charcot-Marie-Tooth disease type 4J"
      },
      {
        "code" : "139518",
        "display" : "Distal hereditary motor neuropathy type 1"
      },
      {
        "code" : "139525",
        "display" : "Distal hereditary motor neuropathy type 2"
      },
      {
        "code" : "139536",
        "display" : "Distal hereditary motor neuropathy type 5"
      },
      {
        "code" : "139547",
        "display" : "Distal spinal muscular atrophy type 3"
      },
      {
        "code" : "139552",
        "display" : "Distal hereditary motor neuropathy, Jerash type"
      },
      {
        "code" : "139557",
        "display" : "X-linked distal spinal muscular atrophy type 3"
      },
      {
        "code" : "139564",
        "display" : "Hereditary sensory and autonomic neuropathy type 1B"
      },
      {
        "code" : "139573",
        "display" : "Hereditary sensory and autonomic neuropathy with deafness and global delay"
      },
      {
        "code" : "139578",
        "display" : "Mutilating hereditary sensory neuropathy with spastic paraplegia"
      },
      {
        "code" : "139583",
        "display" : "X-linked hereditary sensory and autonomic neuropathy with deafness"
      },
      {
        "code" : "139589",
        "display" : "Distal hereditary motor neuropathy type 7"
      },
      {
        "code" : "1397",
        "display" : "Hydrocephaly-cerebellar agenesis syndrome"
      },
      {
        "code" : "1398",
        "display" : "Isolated cerebellar agenesis"
      },
      {
        "code" : "1399",
        "display" : "Richards-Rundle syndrome"
      },
      {
        "code" : "14",
        "display" : "Abetalipoproteinemia"
      },
      {
        "code" : "140",
        "display" : "Campomelic dysplasia"
      },
      {
        "code" : "1401",
        "display" : "CHAND syndrome"
      },
      {
        "code" : "140286",
        "display" : "Secondary hypoparathyroidism due to impaired parathormon secretion"
      },
      {
        "code" : "140436",
        "display" : "Primary intraosseous venous malformation"
      },
      {
        "code" : "140481",
        "display" : "Autosomal dominant slowed nerve conduction velocity"
      },
      {
        "code" : "1406",
        "display" : "Charlie M syndrome"
      },
      {
        "code" : "140896",
        "display" : "Severe acute respiratory syndrome"
      },
      {
        "code" : "140905",
        "display" : "Hyperlipidemia due to hepatic triacylglycerol lipase deficiency"
      },
      {
        "code" : "140908",
        "display" : "Brachydactyly type B2"
      },
      {
        "code" : "140917",
        "display" : "Stapes ankylosis with broad thumbs and toes"
      },
      {
        "code" : "140922",
        "display" : "Titin-related limb-girdle muscular dystrophy R10"
      },
      {
        "code" : "140927",
        "display" : "Self-limited neonatal-infantile epilepsy"
      },
      {
        "code" : "140933",
        "display" : "Linear atrophoderma of Moulin"
      },
      {
        "code" : "140936",
        "display" : "Lelis syndrome"
      },
      {
        "code" : "140941",
        "display" : "Short stature due to primary acid-labile subunit deficiency"
      },
      {
        "code" : "140944",
        "display" : "CLOVES syndrome"
      },
      {
        "code" : "140949",
        "display" : "Low-flow priapism"
      },
      {
        "code" : "140952",
        "display" : "Syndactyly-telecanthus-anogenital and renal malformations syndrome"
      },
      {
        "code" : "140957",
        "display" : "Autosomal dominant macrothrombocytopenia"
      },
      {
        "code" : "140963",
        "display" : "Bilateral microtia-deafness-cleft palate syndrome"
      },
      {
        "code" : "140966",
        "display" : "Palmoplantar keratoderma, Nagashima type"
      },
      {
        "code" : "140969",
        "display" : "Saldino-Mainzer syndrome"
      },
      {
        "code" : "140976",
        "display" : "RHYNS syndrome"
      },
      {
        "code" : "140989",
        "display" : "Primary angiitis of the central nervous system"
      },
      {
        "code" : "141",
        "display" : "Canavan disease"
      },
      {
        "code" : "1410",
        "display" : "Uncombable hair syndrome"
      },
      {
        "code" : "141000",
        "display" : "Orofaciodigital syndrome type 11"
      },
      {
        "code" : "141007",
        "display" : "Orofaciodigital syndrome type 9"
      },
      {
        "code" : "141013",
        "display" : "First branchial cleft anomaly"
      },
      {
        "code" : "141022",
        "display" : "Second branchial cleft anomaly"
      },
      {
        "code" : "141030",
        "display" : "Third branchial cleft anomaly"
      },
      {
        "code" : "141037",
        "display" : "Fourth branchial cleft anomaly"
      },
      {
        "code" : "141046",
        "display" : "Cervical dermoid cyst"
      },
      {
        "code" : "141051",
        "display" : "Facial dermoid cyst"
      },
      {
        "code" : "141061",
        "display" : "Commissural lip fistula"
      },
      {
        "code" : "141064",
        "display" : "Isolated lower lip fistula"
      },
      {
        "code" : "141067",
        "display" : "Cervicofacial fibrochondroma"
      },
      {
        "code" : "141071",
        "display" : "Isolated digestive duplication cyst of the tongue"
      },
      {
        "code" : "141074",
        "display" : "External auditory canal aplasia/hypoplasia"
      },
      {
        "code" : "141077",
        "display" : "Epignathus"
      },
      {
        "code" : "141083",
        "display" : "Nasolacrimal duct cyst"
      },
      {
        "code" : "141091",
        "display" : "Polyrrhinia"
      },
      {
        "code" : "141096",
        "display" : "Supernumerary nostril"
      },
      {
        "code" : "141099",
        "display" : "Proboscis lateralis"
      },
      {
        "code" : "141103",
        "display" : "Nasal dermoid cyst"
      },
      {
        "code" : "141107",
        "display" : "Nasopharyngeal teratoma"
      },
      {
        "code" : "141112",
        "display" : "Nasal glial heterotopia"
      },
      {
        "code" : "141115",
        "display" : "Nasal ganglioglioma"
      },
      {
        "code" : "141118",
        "display" : "Nasal encephalocele"
      },
      {
        "code" : "141121",
        "display" : "Congenital subglottic stenosis"
      },
      {
        "code" : "141124",
        "display" : "Congenital laryngeal cyst"
      },
      {
        "code" : "141127",
        "display" : "Congenital tracheal stenosis"
      },
      {
        "code" : "141132",
        "display" : "Oculo-auriculo-vertebral spectrum"
      },
      {
        "code" : "141145",
        "display" : "Hemifacial hyperplasia"
      },
      {
        "code" : "141148",
        "display" : "Hemifacial myohyperplasia"
      },
      {
        "code" : "141152",
        "display" : "Isolated congenital hypoglossia/aglossia"
      },
      {
        "code" : "141163",
        "display" : "Glossopalatine ankylosis"
      },
      {
        "code" : "141168",
        "display" : "Frontonasal arteriovenous malformation"
      },
      {
        "code" : "141171",
        "display" : "Maxillary arteriovenous malformation"
      },
      {
        "code" : "141174",
        "display" : "Mandibular arteriovenous malformation"
      },
      {
        "code" : "141179",
        "display" : "Non-involuting congenital hemangioma"
      },
      {
        "code" : "141184",
        "display" : "Rapidly involuting congenital hemangioma"
      },
      {
        "code" : "141189",
        "display" : "Cerebrofacial arteriovenous metameric syndrome"
      },
      {
        "code" : "141194",
        "display" : "Cerebrofacial arteriovenous metameric syndrome type 1"
      },
      {
        "code" : "141199",
        "display" : "Cerebrofacial arteriovenous metameric syndrome type 3"
      },
      {
        "code" : "1412",
        "display" : "Tarsal-carpal coalition syndrome"
      },
      {
        "code" : "141209",
        "display" : "Diffuse lymphatic malformation"
      },
      {
        "code" : "141214",
        "display" : "Isolated congenital syngnathia"
      },
      {
        "code" : "141219",
        "display" : "Nasal dorsum fistula"
      },
      {
        "code" : "141239",
        "display" : "Median cleft of the upper lip and maxilla"
      },
      {
        "code" : "141242",
        "display" : "Paramedian nasal cleft"
      },
      {
        "code" : "141258",
        "display" : "Tessier number 4 facial cleft"
      },
      {
        "code" : "141261",
        "display" : "Tessier number 5 facial cleft"
      },
      {
        "code" : "141265",
        "display" : "Tessier number 6 facial cleft"
      },
      {
        "code" : "141276",
        "display" : "Tessier number 7 facial cleft"
      },
      {
        "code" : "141288",
        "display" : "Midline cervical cleft"
      },
      {
        "code" : "141291",
        "display" : "Cleft lip and alveolus"
      },
      {
        "code" : "141333",
        "display" : "Biemond syndrome type 2"
      },
      {
        "code" : "1414",
        "display" : "Cholestasis-lymphedema syndrome"
      },
      {
        "code" : "1415",
        "display" : "Hardikar syndrome"
      },
      {
        "code" : "1416",
        "display" : "Familial calcium pyrophosphate deposition"
      },
      {
        "code" : "142",
        "display" : "Anaplastic thyroid carcinoma"
      },
      {
        "code" : "1422",
        "display" : "Chondrodysplasia-difference of sex development syndrome"
      },
      {
        "code" : "1423",
        "display" : "Lethal recessive chondrodysplasia"
      },
      {
        "code" : "1425",
        "display" : "Desbuquois syndrome"
      },
      {
        "code" : "1426",
        "display" : "Greenberg dysplasia"
      },
      {
        "code" : "1427",
        "display" : "Autosomal recessive otospondylomegaepiphyseal dysplasia"
      },
      {
        "code" : "1429",
        "display" : "Benign hereditary chorea"
      },
      {
        "code" : "143",
        "display" : "Parathyroid carcinoma"
      },
      {
        "code" : "1433",
        "display" : "Choroidal atrophy-alopecia syndrome"
      },
      {
        "code" : "1435",
        "display" : "Xq21 microdeletion syndrome"
      },
      {
        "code" : "1436",
        "display" : "X-linked skeletal dysplasia-intellectual disability syndrome"
      },
      {
        "code" : "1437",
        "display" : "Ring chromosome 1 syndrome"
      },
      {
        "code" : "1438",
        "display" : "Ring chromosome 10 syndrome"
      },
      {
        "code" : "1439",
        "display" : "Ring chromosome 12 syndrome"
      },
      {
        "code" : "144",
        "display" : "Lynch syndrome"
      },
      {
        "code" : "1440",
        "display" : "Ring chromosome 14 syndrome"
      },
      {
        "code" : "1441",
        "display" : "Ring chromosome 17 syndrome"
      },
      {
        "code" : "1442",
        "display" : "Ring chromosome 18 syndrome"
      },
      {
        "code" : "1443",
        "display" : "Ring chromosome 19 syndrome"
      },
      {
        "code" : "1444",
        "display" : "Ring chromosome 20 syndrome"
      },
      {
        "code" : "1445",
        "display" : "Ring chromosome 21 syndrome"
      },
      {
        "code" : "1446",
        "display" : "Ring chromosome 22 syndrome"
      },
      {
        "code" : "1447",
        "display" : "Ring chromosome 4 syndrome"
      },
      {
        "code" : "1448",
        "display" : "Ring chromosome 6 syndrome"
      },
      {
        "code" : "1449",
        "display" : "Ring chromosome 7 syndrome"
      },
      {
        "code" : "145",
        "display" : "Hereditary breast and/or ovarian cancer syndrome"
      },
      {
        "code" : "1450",
        "display" : "Ring chromosome 8 syndrome"
      },
      {
        "code" : "1451",
        "display" : "CINCA syndrome"
      },
      {
        "code" : "1452",
        "display" : "Cleidocranial dysplasia"
      },
      {
        "code" : "1453",
        "display" : "Cleidorhizomelic syndrome"
      },
      {
        "code" : "1454",
        "display" : "Joubert syndrome with hepatic defect"
      },
      {
        "code" : "1456",
        "display" : "Middle aortic syndrome"
      },
      {
        "code" : "1457",
        "display" : "Aorta coarctation"
      },
      {
        "code" : "1458",
        "display" : "CODAS syndrome"
      },
      {
        "code" : "1459",
        "display" : "Celiac disease-epilepsy-cerebral calcification syndrome"
      },
      {
        "code" : "146",
        "display" : "Differentiated thyroid carcinoma"
      },
      {
        "code" : "1460",
        "display" : "Isolated complex III deficiency"
      },
      {
        "code" : "1461",
        "display" : "Criss-cross heart"
      },
      {
        "code" : "1464",
        "display" : "Univentricular heart"
      },
      {
        "code" : "1465",
        "display" : "Coffin-Siris syndrome"
      },
      {
        "code" : "1466",
        "display" : "COFS syndrome"
      },
      {
        "code" : "1467",
        "display" : "Cogan syndrome"
      },
      {
        "code" : "147",
        "display" : "Carbamoyl-phosphate synthetase 1 deficiency"
      },
      {
        "code" : "1471",
        "display" : "Coloboma of macula-brachydactyly type B syndrome"
      },
      {
        "code" : "1473",
        "display" : "Uveal coloboma-cleft lip and palate-intellectual disability"
      },
      {
        "code" : "1475",
        "display" : "Renal coloboma syndrome"
      },
      {
        "code" : "1478",
        "display" : "Interatrial communication"
      },
      {
        "code" : "1479",
        "display" : "Atrial septal defect-atrioventricular conduction defects syndrome"
      },
      {
        "code" : "1482",
        "display" : "Gonococcal conjunctivitis"
      },
      {
        "code" : "1484",
        "display" : "Contractures-ectodermal dysplasia-cleft lip/palate syndrome"
      },
      {
        "code" : "1485",
        "display" : "Arthrogryposis-hyperkeratosis syndrome, lethal form"
      },
      {
        "code" : "1486",
        "display" : "Lethal congenital contracture syndrome type 1"
      },
      {
        "code" : "1487",
        "display" : "Cooks syndrome"
      },
      {
        "code" : "1488",
        "display" : "Cooper-Jabs syndrome"
      },
      {
        "code" : "1489",
        "display" : "Whooping cough"
      },
      {
        "code" : "1490",
        "display" : "Corneal dystrophy-perceptive deafness syndrome"
      },
      {
        "code" : "1493",
        "display" : "Vici syndrome"
      },
      {
        "code" : "1495",
        "display" : "Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome"
      },
      {
        "code" : "1496",
        "display" : "Corpus callosum agenesis-neuronopathy syndrome"
      },
      {
        "code" : "1497",
        "display" : "X-linked complicated corpus callosum dysgenesis"
      },
      {
        "code" : "15",
        "display" : "Achondroplasia"
      },
      {
        "code" : "150",
        "display" : "Nasopharyngeal carcinoma"
      },
      {
        "code" : "1501",
        "display" : "Adrenocortical carcinoma"
      },
      {
        "code" : "1506",
        "display" : "Thin ribs-tubular bones-dysmorphism syndrome"
      },
      {
        "code" : "1507",
        "display" : "Autosomal recessive Robinow syndrome"
      },
      {
        "code" : "1508",
        "display" : "Coxoauricular syndrome"
      },
      {
        "code" : "1509",
        "display" : "Coxopodopatellar syndrome"
      },
      {
        "code" : "1512",
        "display" : "Crane-Heise syndrome"
      },
      {
        "code" : "1513",
        "display" : "Craniodiaphyseal dysplasia"
      },
      {
        "code" : "1514",
        "display" : "Craniodigital-intellectual disability syndrome"
      },
      {
        "code" : "1515",
        "display" : "Cranioectodermal dysplasia"
      },
      {
        "code" : "1516",
        "display" : "Non-syndromic bilambdoid and sagittal craniosynostosis"
      },
      {
        "code" : "1517",
        "display" : "Cantú syndrome"
      },
      {
        "code" : "1519",
        "display" : "SPECC1L-related hypertelorism syndrome"
      },
      {
        "code" : "1520",
        "display" : "Craniofrontonasal dysplasia"
      },
      {
        "code" : "1521",
        "display" : "Craniofrontonasal dysplasia-Poland anomaly syndrome"
      },
      {
        "code" : "1522",
        "display" : "Craniometaphyseal dysplasia"
      },
      {
        "code" : "1524",
        "display" : "Craniomicromelic syndrome"
      },
      {
        "code" : "1525",
        "display" : "Cranio-osteoarthropathy"
      },
      {
        "code" : "1527",
        "display" : "Craniosynostosis, Philadelphia type"
      },
      {
        "code" : "1528",
        "display" : "Craniotelencephalic dysplasia"
      },
      {
        "code" : "1529",
        "display" : "Craniofacial-deafness-hand syndrome"
      },
      {
        "code" : "1532",
        "display" : "Gómez-López-Hernández syndrome"
      },
      {
        "code" : "1538",
        "display" : "Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome"
      },
      {
        "code" : "154",
        "display" : "Familial isolated dilated cardiomyopathy"
      },
      {
        "code" : "1540",
        "display" : "Jackson-Weiss syndrome"
      },
      {
        "code" : "1541",
        "display" : "Craniosynostosis, Boston type"
      },
      {
        "code" : "1544",
        "display" : "Benign focal seizures of adolescence"
      },
      {
        "code" : "1545",
        "display" : "Crisponi syndrome"
      },
      {
        "code" : "1546",
        "display" : "Cryptococcosis"
      },
      {
        "code" : "1547",
        "display" : "Cryptomicrotia-brachydactyly-excess fingertip arch syndrome"
      },
      {
        "code" : "1548",
        "display" : "Cryptorchidism-arachnodactyly-intellectual disability syndrome"
      },
      {
        "code" : "1551",
        "display" : "Familial benign copper deficiency"
      },
      {
        "code" : "1552",
        "display" : "Currarino syndrome"
      },
      {
        "code" : "1553",
        "display" : "Curry-Jones syndrome"
      },
      {
        "code" : "1555",
        "display" : "Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome"
      },
      {
        "code" : "1556",
        "display" : "Cutis marmorata telangiectatica congenita"
      },
      {
        "code" : "155838",
        "display" : "Pinnae fistula or cyst"
      },
      {
        "code" : "155878",
        "display" : "Submucosal cleft palate"
      },
      {
        "code" : "155884",
        "display" : "Coloboma of superior eyelid"
      },
      {
        "code" : "155889",
        "display" : "Coloboma of inferior eyelid"
      },
      {
        "code" : "156",
        "display" : "Carnitine palmitoyl transferase 1A deficiency"
      },
      {
        "code" : "1560",
        "display" : "Cysticercosis"
      },
      {
        "code" : "1561",
        "display" : "Fatal infantile cytochrome C oxidase deficiency"
      },
      {
        "code" : "1563",
        "display" : "Dahlberg-Borer-Newcomer syndrome"
      },
      {
        "code" : "1566",
        "display" : "Dandy-Walker malformation-postaxial polydactyly syndrome"
      },
      {
        "code" : "156728",
        "display" : "Spondyloepimetaphyseal dysplasia, matrilin-3 type"
      },
      {
        "code" : "156731",
        "display" : "Dyssegmental dysplasia, Rolland-Desbuquois type"
      },
      {
        "code" : "1568",
        "display" : "X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome"
      },
      {
        "code" : "157",
        "display" : "Carnitine palmitoyltransferase II deficiency"
      },
      {
        "code" : "1570",
        "display" : "Symbrachydactyly of hands and feet"
      },
      {
        "code" : "1571",
        "display" : "Knobloch syndrome"
      },
      {
        "code" : "157215",
        "display" : "Hereditary hypophosphatemic rickets with hypercalciuria"
      },
      {
        "code" : "1573",
        "display" : "Hypotrichosis with juvenile macular degeneration"
      },
      {
        "code" : "1574",
        "display" : "Retinal degeneration-nanophthalmos-glaucoma syndrome"
      },
      {
        "code" : "157713",
        "display" : "Congenital or early infantile CACH syndrome"
      },
      {
        "code" : "157716",
        "display" : "Late infantile CACH syndrome"
      },
      {
        "code" : "157719",
        "display" : "Juvenile or adult CACH syndrome"
      },
      {
        "code" : "157769",
        "display" : "Situs ambiguus"
      },
      {
        "code" : "157791",
        "display" : "Epithelioid hemangioendothelioma"
      },
      {
        "code" : "157794",
        "display" : "Hereditary mixed polyposis syndrome"
      },
      {
        "code" : "157798",
        "display" : "Serrated polyposis syndrome"
      },
      {
        "code" : "1578",
        "display" : "Pterin-4 alpha-carbinolamine dehydratase deficiency"
      },
      {
        "code" : "157801",
        "display" : "Mesoaxial synostotic syndactyly with phalangeal reduction"
      },
      {
        "code" : "157808",
        "display" : "Isolated pseudoarthrosis of the limbs"
      },
      {
        "code" : "157820",
        "display" : "Cold-induced sweating syndrome"
      },
      {
        "code" : "157823",
        "display" : "Klüver-Bucy syndrome"
      },
      {
        "code" : "157826",
        "display" : "Congenital epulis"
      },
      {
        "code" : "157832",
        "display" : "Craniorhiny"
      },
      {
        "code" : "157835",
        "display" : "Paroxysmal hemicrania"
      },
      {
        "code" : "157846",
        "display" : "Neuroferritinopathy"
      },
      {
        "code" : "157850",
        "display" : "Pantothenate kinase-associated neurodegeneration"
      },
      {
        "code" : "157941",
        "display" : "Huntington disease-like 1"
      },
      {
        "code" : "157946",
        "display" : "Huntington disease-like 3"
      },
      {
        "code" : "157949",
        "display" : "Combined immunodeficiency with granulomatosis"
      },
      {
        "code" : "157954",
        "display" : "ANE syndrome"
      },
      {
        "code" : "157962",
        "display" : "Oculoauricular syndrome, Schorderet type"
      },
      {
        "code" : "157965",
        "display" : "SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome"
      },
      {
        "code" : "157973",
        "display" : "Congenital muscular dystrophy due to LMNA mutation"
      },
      {
        "code" : "157991",
        "display" : "Generalized eruptive histiocytosis"
      },
      {
        "code" : "157997",
        "display" : "Benign cephalic histiocytosis"
      },
      {
        "code" : "158",
        "display" : "Systemic primary carnitine deficiency"
      },
      {
        "code" : "158000",
        "display" : "Juvenile xanthogranuloma"
      },
      {
        "code" : "158003",
        "display" : "Xanthoma disseminatum"
      },
      {
        "code" : "158008",
        "display" : "Papular xanthoma"
      },
      {
        "code" : "158011",
        "display" : "Necrobiotic xanthogranuloma"
      },
      {
        "code" : "158014",
        "display" : "Rosaï-Dorfman disease"
      },
      {
        "code" : "158019",
        "display" : "Indeterminate cell histiocytosis"
      },
      {
        "code" : "158022",
        "display" : "Progressive nodular histiocytosis"
      },
      {
        "code" : "158025",
        "display" : "Hereditary progressive mucinous histiocytosis"
      },
      {
        "code" : "158048",
        "display" : "Hemophagocytic syndrome associated with an infection"
      },
      {
        "code" : "158057",
        "display" : "Acquired hemophagocytic lymphohistiocytosis associated with malignant disease"
      },
      {
        "code" : "158061",
        "display" : "Macrophage activation syndrome"
      },
      {
        "code" : "1581",
        "display" : "Non-distal deletion 10q syndrome"
      },
      {
        "code" : "158668",
        "display" : "Ectodermal dysplasia-skin fragility syndrome"
      },
      {
        "code" : "158673",
        "display" : "Localized dystrophic epidermolysis bullosa, acral form"
      },
      {
        "code" : "158676",
        "display" : "Localized dystrophic epidermolysis bullosa, nails only"
      },
      {
        "code" : "158681",
        "display" : "Epidermolysis bullosa simplex with circinate migratory erythema"
      },
      {
        "code" : "158684",
        "display" : "Epidermolysis bullosa simplex with pyloric atresia"
      },
      {
        "code" : "158687",
        "display" : "Lethal acantholytic erosive disorder"
      },
      {
        "code" : "1587",
        "display" : "Monosomy 13q14 syndrome"
      },
      {
        "code" : "158766",
        "display" : "Typical urticaria pigmentosa"
      },
      {
        "code" : "158769",
        "display" : "Plaque-form urticaria pigmentosa"
      },
      {
        "code" : "158772",
        "display" : "Nodular urticaria pigmentosa"
      },
      {
        "code" : "158775",
        "display" : "Smoldering systemic mastocytosis"
      },
      {
        "code" : "158778",
        "display" : "Isolated bone marrow mastocytosis"
      },
      {
        "code" : "159",
        "display" : "Carnitine-acylcarnitine translocase deficiency"
      },
      {
        "code" : "1590",
        "display" : "Distal deletion 13q syndrome"
      },
      {
        "code" : "1596",
        "display" : "Distal deletion 15q syndrome"
      },
      {
        "code" : "1597",
        "display" : "Distal deletion 17q syndrome"
      },
      {
        "code" : "1598",
        "display" : "Monosomy 18p syndrome"
      },
      {
        "code" : "16",
        "display" : "Blue cone monochromatism"
      },
      {
        "code" : "160",
        "display" : "Castleman disease"
      },
      {
        "code" : "1600",
        "display" : "Monosomy 18q syndrome"
      },
      {
        "code" : "160148",
        "display" : "Cap polyposis"
      },
      {
        "code" : "1606",
        "display" : "1p36 deletion syndrome"
      },
      {
        "code" : "1617",
        "display" : "Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion"
      },
      {
        "code" : "162",
        "display" : "Congenital cataract-anterior segment dysgenesis syndrome"
      },
      {
        "code" : "1620",
        "display" : "Distal deletion 3p syndrome"
      },
      {
        "code" : "1621",
        "display" : "3q13 microdeletion syndrome"
      },
      {
        "code" : "162516",
        "display" : "Isolated congenital nasal pyriform aperture stenosis"
      },
      {
        "code" : "162526",
        "display" : "Isolated congenital auditory ossicle malformation"
      },
      {
        "code" : "1627",
        "display" : "Deletion 5q35 syndrome"
      },
      {
        "code" : "163",
        "display" : "Hereditary hyperferritinemia-cataract syndrome"
      },
      {
        "code" : "163525",
        "display" : "Subacute cutaneous lupus erythematosus"
      },
      {
        "code" : "163596",
        "display" : "Hb Bart's hydrops fetalis"
      },
      {
        "code" : "1636",
        "display" : "Distal monosomy 7q36 syndrome"
      },
      {
        "code" : "163634",
        "display" : "Maffucci syndrome"
      },
      {
        "code" : "163649",
        "display" : "Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome"
      },
      {
        "code" : "163654",
        "display" : "Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome"
      },
      {
        "code" : "163662",
        "display" : "Spondyloepiphyseal dysplasia, Reardon type"
      },
      {
        "code" : "163665",
        "display" : "Spondyloepiphyseal dysplasia tarda, Kohn type"
      },
      {
        "code" : "163668",
        "display" : "Spondyloepiphyseal dysplasia, MacDermot type"
      },
      {
        "code" : "163681",
        "display" : "CNTNAP2-related developmental and epileptic encephalopathy"
      },
      {
        "code" : "163684",
        "display" : "Leukoencephalopathy-dystonia-motor neuropathy syndrome"
      },
      {
        "code" : "163690",
        "display" : "Hypotonia-cystinuria syndrome"
      },
      {
        "code" : "163693",
        "display" : "2p21 microdeletion syndrome"
      },
      {
        "code" : "163696",
        "display" : "Action myoclonus-renal failure syndrome"
      },
      {
        "code" : "163699",
        "display" : "Alveolar soft tissue sarcoma"
      },
      {
        "code" : "163703",
        "display" : "Febrile infection-related epilepsy syndrome"
      },
      {
        "code" : "163708",
        "display" : "Cryptogenic late-onset epileptic spasms"
      },
      {
        "code" : "163717",
        "display" : "Familial mesial temporal lobe epilepsy"
      },
      {
        "code" : "163721",
        "display" : "Rolandic epilepsy-speech dyspraxia syndrome"
      },
      {
        "code" : "163727",
        "display" : "Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome"
      },
      {
        "code" : "163746",
        "display" : "Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease"
      },
      {
        "code" : "163921",
        "display" : "Posttransplant acute limbic encephalitis"
      },
      {
        "code" : "163927",
        "display" : "Pustulosis palmaris et plantaris"
      },
      {
        "code" : "163931",
        "display" : "Acrodermatitis continua of Hallopeau"
      },
      {
        "code" : "163934",
        "display" : "Atopic keratoconjunctivitis"
      },
      {
        "code" : "163937",
        "display" : "X-linked intellectual disability, Najm type"
      },
      {
        "code" : "163956",
        "display" : "X-linked intellectual disability, Nascimento type"
      },
      {
        "code" : "163961",
        "display" : "X-linked cerebral-cerebellar-coloboma syndrome"
      },
      {
        "code" : "163966",
        "display" : "X-linked dominant chondrodysplasia, Chassaing-Lacombe type"
      },
      {
        "code" : "163971",
        "display" : "X-linked intellectual disability, Cilliers type"
      },
      {
        "code" : "163976",
        "display" : "X-linked intellectual disability, Van Esch type"
      },
      {
        "code" : "163979",
        "display" : "X-linked intellectual disability-craniofacioskeletal syndrome"
      },
      {
        "code" : "163985",
        "display" : "Hyperekplexia-epilepsy syndrome"
      },
      {
        "code" : "1642",
        "display" : "Distal deletion 9p syndrome"
      },
      {
        "code" : "1643",
        "display" : "Xp22.3 microdeletion syndrome"
      },
      {
        "code" : "1646",
        "display" : "Chromosome Y microdeletion syndrome"
      },
      {
        "code" : "1647",
        "display" : "Oculocerebrocutaneous syndrome"
      },
      {
        "code" : "164726",
        "display" : "Acute myeloid leukemia and myelodysplastic syndromes related to radiation"
      },
      {
        "code" : "164736",
        "display" : "Familial advanced sleep-phase syndrome"
      },
      {
        "code" : "1652",
        "display" : "Dent disease"
      },
      {
        "code" : "1653",
        "display" : "Dentin dysplasia"
      },
      {
        "code" : "1655",
        "display" : "Müllerian derivatives-lymphangiectasia-polydactyly syndrome"
      },
      {
        "code" : "1656",
        "display" : "Dermatitis herpetiformis"
      },
      {
        "code" : "1657",
        "display" : "Dermatoosteolysis, Kirghizian type"
      },
      {
        "code" : "1658",
        "display" : "Absence of fingerprints-congenital milia syndrome"
      },
      {
        "code" : "1659",
        "display" : "Dermatoleukodystrophy"
      },
      {
        "code" : "165955",
        "display" : "Wound myiasis"
      },
      {
        "code" : "165958",
        "display" : "Cavitary myiasis"
      },
      {
        "code" : "165991",
        "display" : "Exercise-induced hyperinsulinism"
      },
      {
        "code" : "1660",
        "display" : "Dermoodontodysplasia"
      },
      {
        "code" : "166002",
        "display" : "Multiple epiphyseal dysplasia due to collagen 9 anomaly"
      },
      {
        "code" : "166016",
        "display" : "Multiple epiphyseal dysplasia, Lowry type"
      },
      {
        "code" : "166024",
        "display" : "Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome"
      },
      {
        "code" : "166029",
        "display" : "Multiple epiphyseal dysplasia-severe proximal femoral dysplasia syndrome"
      },
      {
        "code" : "166032",
        "display" : "Multiple epiphyseal dysplasia-miniepiphyses syndrome"
      },
      {
        "code" : "166035",
        "display" : "Brachydactyly-short stature-retinitis pigmentosa syndrome"
      },
      {
        "code" : "166038",
        "display" : "Metaphyseal chondrodysplasia, Kaitila type"
      },
      {
        "code" : "166063",
        "display" : "Pontocerebellar hypoplasia type 4"
      },
      {
        "code" : "166073",
        "display" : "Pontocerebellar hypoplasia type 6"
      },
      {
        "code" : "166078",
        "display" : "Von Willebrand disease type 1"
      },
      {
        "code" : "166081",
        "display" : "Von Willebrand disease type 2"
      },
      {
        "code" : "166084",
        "display" : "Von Willebrand disease type 2A"
      },
      {
        "code" : "166087",
        "display" : "Von Willebrand disease type 2B"
      },
      {
        "code" : "166090",
        "display" : "Von Willebrand disease type 2M"
      },
      {
        "code" : "166093",
        "display" : "Von Willebrand disease type 2N"
      },
      {
        "code" : "166096",
        "display" : "Von Willebrand disease type 3"
      },
      {
        "code" : "1661",
        "display" : "X-linked corneal dermoid"
      },
      {
        "code" : "166100",
        "display" : "Autosomal dominant otospondylomegaepiphyseal dysplasia"
      },
      {
        "code" : "166105",
        "display" : "FASTKD2-related infantile mitochondrial encephalomyopathy"
      },
      {
        "code" : "166108",
        "display" : "Birk-Barel syndrome"
      },
      {
        "code" : "166113",
        "display" : "Bazex syndrome"
      },
      {
        "code" : "166119",
        "display" : "Isolated osteopoikilosis"
      },
      {
        "code" : "1662",
        "display" : "Restrictive dermopathy"
      },
      {
        "code" : "166260",
        "display" : "Dentinogenesis imperfecta type 2"
      },
      {
        "code" : "166265",
        "display" : "Dentinogenesis imperfecta type 3"
      },
      {
        "code" : "166272",
        "display" : "Odontochondrodysplasia"
      },
      {
        "code" : "166277",
        "display" : "Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia"
      },
      {
        "code" : "166282",
        "display" : "Hereditary sick sinus syndrome"
      },
      {
        "code" : "166286",
        "display" : "Porokeratotic eccrine ostial and dermal duct nevus"
      },
      {
        "code" : "166291",
        "display" : "Dirofilariasis"
      },
      {
        "code" : "166308",
        "display" : "Benign infantile focal epilepsy with midline spikes and waves during sleep"
      },
      {
        "code" : "166409",
        "display" : "Photosensitive occipital lobe epilepsy"
      },
      {
        "code" : "166412",
        "display" : "Hot water reflex epilepsy"
      },
      {
        "code" : "166415",
        "display" : "Audiogenic seizures"
      },
      {
        "code" : "166418",
        "display" : "Eating reflex epilepsy"
      },
      {
        "code" : "166421",
        "display" : "Orgasm-induced seizures"
      },
      {
        "code" : "166424",
        "display" : "Thinking seizures"
      },
      {
        "code" : "166427",
        "display" : "Startle epilepsy"
      },
      {
        "code" : "166430",
        "display" : "Micturation-induced seizures"
      },
      {
        "code" : "166433",
        "display" : "Epilepsy with reading-induced seizures"
      },
      {
        "code" : "1665",
        "display" : "Sporadic fetal brain disruption sequence"
      },
      {
        "code" : "1666",
        "display" : "Dextrocardia"
      },
      {
        "code" : "1667",
        "display" : "Wolcott-Rallison syndrome"
      },
      {
        "code" : "167",
        "display" : "Chédiak-Higashi syndrome"
      },
      {
        "code" : "1670",
        "display" : "Chronic diarrhea with villous atrophy"
      },
      {
        "code" : "1671",
        "display" : "Split cord malformation type I"
      },
      {
        "code" : "1672",
        "display" : "Diencephalic syndrome"
      },
      {
        "code" : "1675",
        "display" : "Dihydropyrimidine dehydrogenase deficiency"
      },
      {
        "code" : "1676",
        "display" : "Idiopathic pulmonary artery dilatation"
      },
      {
        "code" : "167635",
        "display" : "Scleromyxedema"
      },
      {
        "code" : "1677",
        "display" : "Familial idiopathic dilatation of the right atrium"
      },
      {
        "code" : "1679",
        "display" : "Diphtheria"
      },
      {
        "code" : "168",
        "display" : "Loose anagen syndrome"
      },
      {
        "code" : "1681",
        "display" : "Diprosopus"
      },
      {
        "code" : "1682",
        "display" : "Arterial dissection-lentiginosis syndrome"
      },
      {
        "code" : "168443",
        "display" : "Spondyloepimetaphyseal dysplasia-hypotrichosis syndrome"
      },
      {
        "code" : "168451",
        "display" : "Spondyloepimetaphyseal dysplasia-abnormal dentition syndrome"
      },
      {
        "code" : "168454",
        "display" : "Spondyloepimetaphyseal dysplasia, Geneviève type"
      },
      {
        "code" : "168544",
        "display" : "Spondylometaphyseal dysplasia, Golden type"
      },
      {
        "code" : "168549",
        "display" : "Axial spondylometaphyseal dysplasia"
      },
      {
        "code" : "168552",
        "display" : "Spondylometaphyseal dysplasia-bowed forearms-facial dysmorphism syndrome"
      },
      {
        "code" : "168555",
        "display" : "Spondylometaphyseal dysplasia, A4 type"
      },
      {
        "code" : "168558",
        "display" : "46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency"
      },
      {
        "code" : "168563",
        "display" : "46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome"
      },
      {
        "code" : "168566",
        "display" : "Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3"
      },
      {
        "code" : "168569",
        "display" : "H syndrome"
      },
      {
        "code" : "168572",
        "display" : "Native American myopathy"
      },
      {
        "code" : "168577",
        "display" : "Hereditary cryohydrocytosis with reduced stomatin"
      },
      {
        "code" : "168583",
        "display" : "Hereditary North American Indian childhood cirrhosis"
      },
      {
        "code" : "168588",
        "display" : "Hyperandrogenism due to cortisone reductase deficiency"
      },
      {
        "code" : "168593",
        "display" : "Sudden infant death-dysgenesis of the testes syndrome"
      },
      {
        "code" : "168598",
        "display" : "Methionine adenosyltransferase I/III deficiency"
      },
      {
        "code" : "1686",
        "display" : "Cardiac diverticulum"
      },
      {
        "code" : "168601",
        "display" : "Congenital enteropathy due to enteropeptidase deficiency"
      },
      {
        "code" : "168606",
        "display" : "Seborrhea-like dermatitis with psoriasiform elements"
      },
      {
        "code" : "168612",
        "display" : "Congenital deficiency in alpha-fetoprotein"
      },
      {
        "code" : "168615",
        "display" : "Hereditary persistence of alpha-fetoprotein"
      },
      {
        "code" : "168621",
        "display" : "Dysplasia of head of femur, Meyer type"
      },
      {
        "code" : "168624",
        "display" : "Familial scaphocephaly syndrome, McGillivray type"
      },
      {
        "code" : "168629",
        "display" : "Autosomal thrombocytopenia with normal platelets"
      },
      {
        "code" : "168632",
        "display" : "Generalized basaloid follicular hamartoma syndrome"
      },
      {
        "code" : "168782",
        "display" : "Childhood disintegrative disorder"
      },
      {
        "code" : "168796",
        "display" : "Heart-hand syndrome, Slovenian type"
      },
      {
        "code" : "168811",
        "display" : "Malignant peritoneal mesothelioma"
      },
      {
        "code" : "168816",
        "display" : "Peritoneal inclusion cyst"
      },
      {
        "code" : "168829",
        "display" : "Primary peritoneal carcinoma"
      },
      {
        "code" : "168940",
        "display" : "Chronic eosinophilic leukemia"
      },
      {
        "code" : "168947",
        "display" : "Myeloid/lymphoid neoplasm associated with PDGFRA rearrangement"
      },
      {
        "code" : "168950",
        "display" : "Myeloid/lymphoid neoplasm associated with PDGFRB rearrangement"
      },
      {
        "code" : "168953",
        "display" : "Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement"
      },
      {
        "code" : "168960",
        "display" : "Refractory anemia with excess blasts in transformation"
      },
      {
        "code" : "168966",
        "display" : "Composite lymphoma"
      },
      {
        "code" : "168984",
        "display" : "CLAPO syndrome"
      },
      {
        "code" : "168999",
        "display" : "Malignant melanoma of the mucosa"
      },
      {
        "code" : "169",
        "display" : "Ringed hair disease"
      },
      {
        "code" : "169079",
        "display" : "Cernunnos-XLF deficiency"
      },
      {
        "code" : "169082",
        "display" : "Combined immunodeficiency due to CD3gamma deficiency"
      },
      {
        "code" : "169085",
        "display" : "Susceptibility to respiratory infections associated with CD8alpha chain mutation"
      },
      {
        "code" : "169090",
        "display" : "Combined immunodeficiency due to CRAC channel dysfunction"
      },
      {
        "code" : "169095",
        "display" : "Severe combined immunodeficiency due to FOXN1 deficiency"
      },
      {
        "code" : "169100",
        "display" : "Immunodeficiency due to CD25 deficiency"
      },
      {
        "code" : "169105",
        "display" : "Good syndrome"
      },
      {
        "code" : "169110",
        "display" : "Immunoglobulin heavy chain deficiency"
      },
      {
        "code" : "169139",
        "display" : "Transient hypogammaglobulinemia of infancy"
      },
      {
        "code" : "169142",
        "display" : "Recurrent infections due to specific granule deficiency"
      },
      {
        "code" : "169147",
        "display" : "Immunodeficiency due to a classical component pathway complement deficiency"
      },
      {
        "code" : "169150",
        "display" : "Immunodeficiency due to a late component of complement deficiency"
      },
      {
        "code" : "169154",
        "display" : "T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency"
      },
      {
        "code" : "169157",
        "display" : "T-B+ severe combined immunodeficiency due to CD45 deficiency"
      },
      {
        "code" : "169160",
        "display" : "T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta"
      },
      {
        "code" : "169186",
        "display" : "Autosomal recessive centronuclear myopathy"
      },
      {
        "code" : "169189",
        "display" : "Autosomal dominant centronuclear myopathy"
      },
      {
        "code" : "1692",
        "display" : "Mosaic trisomy 1 syndrome"
      },
      {
        "code" : "169464",
        "display" : "Primary CD59 deficiency"
      },
      {
        "code" : "169467",
        "display" : "Recurrent Neisseria infections due to factor D deficiency"
      },
      {
        "code" : "1695",
        "display" : "Non-distal duplication 10q syndrome"
      },
      {
        "code" : "169793",
        "display" : "Severe hemophilia B"
      },
      {
        "code" : "169796",
        "display" : "Moderate hemophilia B"
      },
      {
        "code" : "169799",
        "display" : "Mild hemophilia B"
      },
      {
        "code" : "1698",
        "display" : "Mosaic trisomy 12 syndrome"
      },
      {
        "code" : "169802",
        "display" : "Severe hemophilia A"
      },
      {
        "code" : "169805",
        "display" : "Moderate hemophilia A"
      },
      {
        "code" : "169808",
        "display" : "Mild hemophilia A"
      },
      {
        "code" : "1699",
        "display" : "Trisomy 12p syndrome"
      },
      {
        "code" : "17",
        "display" : "Fatal infantile lactic acidosis with methylmalonic aciduria"
      },
      {
        "code" : "170",
        "display" : "Woolly hair"
      },
      {
        "code" : "1702",
        "display" : "Non-distal duplication 13q syndrome"
      },
      {
        "code" : "1703",
        "display" : "Mosaic trisomy 14 syndrome"
      },
      {
        "code" : "1705",
        "display" : "Distal duplication 14q syndrome"
      },
      {
        "code" : "1706",
        "display" : "Mosaic trisomy 15 syndrome"
      },
      {
        "code" : "1707",
        "display" : "Distal duplication 15q syndrome"
      },
      {
        "code" : "1708",
        "display" : "Mosaic trisomy 16 syndrome"
      },
      {
        "code" : "171",
        "display" : "Primary sclerosing cholangitis"
      },
      {
        "code" : "1711",
        "display" : "Mosaic trisomy 17 syndrome"
      },
      {
        "code" : "171220",
        "display" : "Isolated rectal duplication"
      },
      {
        "code" : "1713",
        "display" : "17p11.2 microduplication syndrome"
      },
      {
        "code" : "171430",
        "display" : "Severe congenital nemaline myopathy"
      },
      {
        "code" : "171433",
        "display" : "Intermediate nemaline myopathy"
      },
      {
        "code" : "171436",
        "display" : "Typical nemaline myopathy"
      },
      {
        "code" : "171439",
        "display" : "Childhood-onset nemaline myopathy"
      },
      {
        "code" : "171442",
        "display" : "Adult-onset nemaline myopathy"
      },
      {
        "code" : "171445",
        "display" : "Muscle filaminopathy"
      },
      {
        "code" : "1715",
        "display" : "Trisomy 18p syndrome"
      },
      {
        "code" : "1716",
        "display" : "Distal duplication 18q syndrome"
      },
      {
        "code" : "171607",
        "display" : "X-linked spastic paraplegia type 34"
      },
      {
        "code" : "171612",
        "display" : "Autosomal dominant spastic paraplegia type 37"
      },
      {
        "code" : "171617",
        "display" : "Autosomal dominant spastic paraplegia type 38"
      },
      {
        "code" : "171622",
        "display" : "Autosomal recessive spastic paraplegia type 32"
      },
      {
        "code" : "171629",
        "display" : "Autosomal recessive spastic paraplegia type 35"
      },
      {
        "code" : "171673",
        "display" : "Limbal stem cell deficiency"
      },
      {
        "code" : "171680",
        "display" : "Lissencephaly due to TUBA1A mutation"
      },
      {
        "code" : "171684",
        "display" : "Idiopathic bilateral vestibulopathy"
      },
      {
        "code" : "171690",
        "display" : "Metabolic myopathy due to lactate transporter defect"
      },
      {
        "code" : "171695",
        "display" : "Parkinsonian-pyramidal syndrome"
      },
      {
        "code" : "1717",
        "display" : "Distal duplication 19q syndrome"
      },
      {
        "code" : "171700",
        "display" : "Diffuse panbronchiolitis"
      },
      {
        "code" : "171703",
        "display" : "Microcephaly-polymicrogyria-corpus callosum agenesis syndrome"
      },
      {
        "code" : "171706",
        "display" : "Short stature-delayed bone age due to thyroid hormone metabolism deficiency"
      },
      {
        "code" : "171709",
        "display" : "Male infertility due to globozoospermia"
      },
      {
        "code" : "171719",
        "display" : "Cutis laxa-Marfanoid syndrome"
      },
      {
        "code" : "171723",
        "display" : "White sponge nevus"
      },
      {
        "code" : "171829",
        "display" : "6q16 microdeletion syndrome"
      },
      {
        "code" : "171839",
        "display" : "Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome"
      },
      {
        "code" : "171844",
        "display" : "Blindness-scoliosis-arachnodactyly syndrome"
      },
      {
        "code" : "171848",
        "display" : "Polyneuropathy-hearing loss-ataxia-retinitis pigmentosa-cataract syndrome"
      },
      {
        "code" : "171851",
        "display" : "MEDNIK syndrome"
      },
      {
        "code" : "171863",
        "display" : "Autosomal dominant spastic paraplegia type 42"
      },
      {
        "code" : "171866",
        "display" : "Spondyloepimetaphyseal dysplasia, aggrecan type"
      },
      {
        "code" : "171871",
        "display" : "Renal pseudohypoaldosteronism type 1"
      },
      {
        "code" : "171876",
        "display" : "Generalized pseudohypoaldosteronism type 1"
      },
      {
        "code" : "171881",
        "display" : "Cap myopathy"
      },
      {
        "code" : "171886",
        "display" : "Cylindrical spirals myopathy"
      },
      {
        "code" : "171889",
        "display" : "Myopathy with hexagonally cross-linked tubular arrays"
      },
      {
        "code" : "171929",
        "display" : "Trisomy 10p syndrome"
      },
      {
        "code" : "172",
        "display" : "Progressive familial intrahepatic cholestasis"
      },
      {
        "code" : "1723",
        "display" : "Mosaic trisomy 2 syndrome"
      },
      {
        "code" : "1724",
        "display" : "Mosaic trisomy 20 syndrome"
      },
      {
        "code" : "1727",
        "display" : "22q11.2 duplication syndrome"
      },
      {
        "code" : "173",
        "display" : "Cholera"
      },
      {
        "code" : "1738",
        "display" : "Trisomy 4p syndrome"
      },
      {
        "code" : "174",
        "display" : "Metaphyseal chondrodysplasia, Schmid type"
      },
      {
        "code" : "1742",
        "display" : "Trisomy 5p syndrome"
      },
      {
        "code" : "1745",
        "display" : "Distal duplication 6p syndrome"
      },
      {
        "code" : "1747",
        "display" : "Mosaic trisomy 7 syndrome"
      },
      {
        "code" : "175",
        "display" : "Cartilage-hair hypoplasia"
      },
      {
        "code" : "1752",
        "display" : "Trisomy 8q syndrome"
      },
      {
        "code" : "1756",
        "display" : "Caudal duplication"
      },
      {
        "code" : "1757",
        "display" : "Fibular dimelia-diplopodia syndrome"
      },
      {
        "code" : "1759",
        "display" : "Thoraco-abdominal enteric duplication"
      },
      {
        "code" : "1762",
        "display" : "Proximal Xq28 duplication syndrome"
      },
      {
        "code" : "1764",
        "display" : "Familial dysautonomia"
      },
      {
        "code" : "1766",
        "display" : "Dysequilibrium syndrome"
      },
      {
        "code" : "1768",
        "display" : "Familial caudal dysgenesis"
      },
      {
        "code" : "177",
        "display" : "Rhizomelic chondrodysplasia punctata"
      },
      {
        "code" : "1770",
        "display" : "XY type gonadal dysgenesis-associated anomalies syndrome"
      },
      {
        "code" : "1772",
        "display" : "45,X/46,XY mixed gonadal dysgenesis"
      },
      {
        "code" : "1775",
        "display" : "Dyskeratosis congenita"
      },
      {
        "code" : "1777",
        "display" : "Temtamy syndrome"
      },
      {
        "code" : "1778",
        "display" : "Facial dysmorphism-shawl scrotum-joint laxity syndrome"
      },
      {
        "code" : "1779",
        "display" : "Dysmorphism-cleft palate-loose skin syndrome"
      },
      {
        "code" : "177901",
        "display" : "Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1"
      },
      {
        "code" : "177904",
        "display" : "Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2"
      },
      {
        "code" : "177907",
        "display" : "Prader-Willi syndrome due to translocation"
      },
      {
        "code" : "177910",
        "display" : "Prader-Willi syndrome due to imprinting mutation"
      },
      {
        "code" : "177926",
        "display" : "Bleeding disorder in hemophilia A carriers"
      },
      {
        "code" : "177929",
        "display" : "Bleeding disorder in hemophilia B carriers"
      },
      {
        "code" : "178",
        "display" : "Chordoma"
      },
      {
        "code" : "1780",
        "display" : "Thakker-Donnai syndrome"
      },
      {
        "code" : "178029",
        "display" : "Arginine vasopressin deficiency"
      },
      {
        "code" : "178145",
        "display" : "Moderate multiminicore disease with hand involvement"
      },
      {
        "code" : "178148",
        "display" : "Antenatal multiminicore disease with arthrogryposis multiplex congenita"
      },
      {
        "code" : "1782",
        "display" : "Dysosteosclerosis"
      },
      {
        "code" : "178303",
        "display" : "8q22.1 microdeletion syndrome"
      },
      {
        "code" : "178307",
        "display" : "Reticulate acropigmentation of Kitamura"
      },
      {
        "code" : "178311",
        "display" : "Isolated sternocostoclavicular hyperostosis"
      },
      {
        "code" : "178315",
        "display" : "Undifferentiated embryonal sarcoma of the liver"
      },
      {
        "code" : "178320",
        "display" : "Acute lung injury"
      },
      {
        "code" : "178333",
        "display" : "Åland Islands eye disease"
      },
      {
        "code" : "178338",
        "display" : "UV-sensitive syndrome"
      },
      {
        "code" : "178342",
        "display" : "Inflammatory myofibroblastic tumor"
      },
      {
        "code" : "178345",
        "display" : "Aromatase excess syndrome"
      },
      {
        "code" : "178355",
        "display" : "Smith-McCort dysplasia"
      },
      {
        "code" : "178364",
        "display" : "Syndromic microphthalmia type 5"
      },
      {
        "code" : "178377",
        "display" : "Osteosclerosis-developmental delay-craniosynostosis syndrome"
      },
      {
        "code" : "178382",
        "display" : "Congenital vertical talus"
      },
      {
        "code" : "178389",
        "display" : "Osteopetrosis-hypogammaglobulinemia syndrome"
      },
      {
        "code" : "178396",
        "display" : "Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation"
      },
      {
        "code" : "1784",
        "display" : "Acrofrontofacionasal dysostosis"
      },
      {
        "code" : "178400",
        "display" : "Distal myopathy with anterior tibial onset"
      },
      {
        "code" : "178461",
        "display" : "X-linked myopathy with postural muscle atrophy"
      },
      {
        "code" : "178464",
        "display" : "Hereditary myopathy with early respiratory failure"
      },
      {
        "code" : "178469",
        "display" : "Autosomal dominant non-syndromic intellectual disability"
      },
      {
        "code" : "178475",
        "display" : "Wound botulism"
      },
      {
        "code" : "178478",
        "display" : "Infant botulism"
      },
      {
        "code" : "178481",
        "display" : "Intestinal botulism"
      },
      {
        "code" : "178487",
        "display" : "Adult intestinal botulism"
      },
      {
        "code" : "178506",
        "display" : "Brain calcification, Rajab type"
      },
      {
        "code" : "178509",
        "display" : "Perry syndrome"
      },
      {
        "code" : "178512",
        "display" : "Folliculotropic mycosis fungoides"
      },
      {
        "code" : "178517",
        "display" : "Localized pagetoid reticulosis"
      },
      {
        "code" : "178522",
        "display" : "Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma"
      },
      {
        "code" : "178528",
        "display" : "Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma"
      },
      {
        "code" : "178533",
        "display" : "Primary cutaneous gamma/delta-positive T-cell lymphoma"
      },
      {
        "code" : "178536",
        "display" : "Primary cutaneous marginal zone B-cell lymphoma"
      },
      {
        "code" : "178540",
        "display" : "Primary cutaneous follicle center lymphoma"
      },
      {
        "code" : "178544",
        "display" : "Primary cutaneous diffuse large B-cell lymphoma, leg type"
      },
      {
        "code" : "1786",
        "display" : "Acrofacial dysostosis, Catania type"
      },
      {
        "code" : "1787",
        "display" : "Acrofacial dysostosis, Palagonia type"
      },
      {
        "code" : "1788",
        "display" : "Acrofacial dysostosis, Rodríguez type"
      },
      {
        "code" : "179",
        "display" : "Birdshot chorioretinopathy"
      },
      {
        "code" : "1790",
        "display" : "Hypomandibular faciocranial dysostosis"
      },
      {
        "code" : "1791",
        "display" : "Frontofacionasal dysplasia"
      },
      {
        "code" : "1794",
        "display" : "Oculomaxillofacial dysostosis"
      },
      {
        "code" : "179490",
        "display" : "Obesity due to congenital leptin resistance"
      },
      {
        "code" : "179494",
        "display" : "Obesity due to leptin receptor gene deficiency"
      },
      {
        "code" : "1797",
        "display" : "Autosomal dominant spondylocostal dysostosis"
      },
      {
        "code" : "1798",
        "display" : "Craniofacial dysostosis-diaphyseal hyperplasia syndrome"
      },
      {
        "code" : "1799",
        "display" : "Familial developmental dysphasia"
      },
      {
        "code" : "18",
        "display" : "Distal renal tubular acidosis"
      },
      {
        "code" : "180",
        "display" : "Choroideremia"
      },
      {
        "code" : "180074",
        "display" : "True unicornuate uterus"
      },
      {
        "code" : "180079",
        "display" : "Pseudounicornuate uterus"
      },
      {
        "code" : "180086",
        "display" : "Didelphys uterus"
      },
      {
        "code" : "1801",
        "display" : "Kyphomelic dysplasia"
      },
      {
        "code" : "180106",
        "display" : "Bicervical bicornuate uterus and blind hemivagina"
      },
      {
        "code" : "180111",
        "display" : "Bicervical bicornuate uterus with patent cervix and vagina"
      },
      {
        "code" : "180114",
        "display" : "Unicervical bicornuate uterus"
      },
      {
        "code" : "180126",
        "display" : "Complete septate uterus"
      },
      {
        "code" : "180129",
        "display" : "Partial septate uterus"
      },
      {
        "code" : "180139",
        "display" : "Uterine hypoplasia"
      },
      {
        "code" : "180142",
        "display" : "Absence of uterine body"
      },
      {
        "code" : "180145",
        "display" : "Uterine cervical aplasia and agenesis"
      },
      {
        "code" : "180154",
        "display" : "Septate vagina"
      },
      {
        "code" : "180157",
        "display" : "Longitudinal vaginal septum"
      },
      {
        "code" : "180160",
        "display" : "Transverse vaginal septum"
      },
      {
        "code" : "180176",
        "display" : "Familial juvenile hypertrophy of the breast"
      },
      {
        "code" : "180182",
        "display" : "Supernumerary breasts"
      },
      {
        "code" : "180188",
        "display" : "Isolated congenital breast hypoplasia/aplasia"
      },
      {
        "code" : "1802",
        "display" : "Ghosal hematodiaphyseal dysplasia"
      },
      {
        "code" : "180226",
        "display" : "Embryonal carcinoma"
      },
      {
        "code" : "180229",
        "display" : "Polyembryoma"
      },
      {
        "code" : "180234",
        "display" : "Mixed germ cell tumor"
      },
      {
        "code" : "180237",
        "display" : "Benign tumor of fallopian tubes"
      },
      {
        "code" : "180242",
        "display" : "Malignant tumor of fallopian tubes"
      },
      {
        "code" : "180247",
        "display" : "Vaginal carcinoma"
      },
      {
        "code" : "180261",
        "display" : "Phyllodes tumor of the breast"
      },
      {
        "code" : "180267",
        "display" : "Giant adenofibroma of the breast"
      },
      {
        "code" : "180275",
        "display" : "Paget disease of the nipple"
      },
      {
        "code" : "1803",
        "display" : "Thoracomelic dysplasia"
      },
      {
        "code" : "1806",
        "display" : "Ectodermal dysplasia-blindness syndrome"
      },
      {
        "code" : "1807",
        "display" : "Focal facial dermal dysplasia type III"
      },
      {
        "code" : "1808",
        "display" : "Hidrotic ectodermal dysplasia, Christianson-Fourie type"
      },
      {
        "code" : "1809",
        "display" : "Hidrotic ectodermal dysplasia, Halal type"
      },
      {
        "code" : "181",
        "display" : "X-linked hypohidrotic ectodermal dysplasia"
      },
      {
        "code" : "1810",
        "display" : "Autosomal dominant hypohidrotic ectodermal dysplasia"
      },
      {
        "code" : "1811",
        "display" : "Odontomicronychial dysplasia"
      },
      {
        "code" : "1812",
        "display" : "Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome"
      },
      {
        "code" : "181428",
        "display" : "Familial Hyperalphalipoproteinemia"
      },
      {
        "code" : "1816",
        "display" : "Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome"
      },
      {
        "code" : "1818",
        "display" : "Ectodermal dysplasia, trichoodontoonychial type"
      },
      {
        "code" : "182",
        "display" : "Chromomycosis"
      },
      {
        "code" : "182050",
        "display" : "MYH9-related syndromic thrombocytopenia"
      },
      {
        "code" : "182127",
        "display" : "Extragonadal germinoma"
      },
      {
        "code" : "1822",
        "display" : "Dysplasia epiphysealis hemimelica"
      },
      {
        "code" : "1824",
        "display" : "Lowry-Wood syndrome"
      },
      {
        "code" : "1825",
        "display" : "Epiphyseal dysplasia-hearing loss-dysmorphism syndrome"
      },
      {
        "code" : "1826",
        "display" : "Frontometaphyseal dysplasia"
      },
      {
        "code" : "1827",
        "display" : "Acromelic frontonasal dysplasia"
      },
      {
        "code" : "183",
        "display" : "Eosinophilic granulomatosis with polyangiitis"
      },
      {
        "code" : "1830",
        "display" : "Schimke immuno-osseous dysplasia"
      },
      {
        "code" : "1832",
        "display" : "Osteosclerotic bone dysplasia"
      },
      {
        "code" : "1834",
        "display" : "Axial mesodermal dysplasia spectrum"
      },
      {
        "code" : "1836",
        "display" : "Mesomelic dysplasia, Kantaputra type"
      },
      {
        "code" : "183663",
        "display" : "Hyper-IgM syndrome with susceptibility to opportunistic infections"
      },
      {
        "code" : "183666",
        "display" : "Hyper-IgM syndrome without susceptibility to opportunistic infections"
      },
      {
        "code" : "183675",
        "display" : "Recurrent infections associated with rare immunoglobulin isotypes deficiency"
      },
      {
        "code" : "183678",
        "display" : "Hermansky-Pudlak syndrome due to AP-3 deficiency"
      },
      {
        "code" : "1837",
        "display" : "Metaphyseal chondrodysplasia, Rosenberg type"
      },
      {
        "code" : "183707",
        "display" : "Infantile LAD-like disease due to RAC2 deficiency"
      },
      {
        "code" : "1839",
        "display" : "Hereditary mucoepithelial dysplasia"
      },
      {
        "code" : "184",
        "display" : "Cherubism"
      },
      {
        "code" : "1842",
        "display" : "Bone dysplasia, lethal Holmgren type"
      },
      {
        "code" : "1848",
        "display" : "Renal agenesis, bilateral"
      },
      {
        "code" : "185",
        "display" : "Scimitar syndrome"
      },
      {
        "code" : "1851",
        "display" : "Multicystic dysplastic kidney"
      },
      {
        "code" : "1852",
        "display" : "X-linked retinal dysplasia"
      },
      {
        "code" : "1855",
        "display" : "Spondyloenchondrodysplasia"
      },
      {
        "code" : "1856",
        "display" : "Spondyloperipheral dysplasia-short ulna syndrome"
      },
      {
        "code" : "1858",
        "display" : "Skeletal dysplasia-epilepsy-short stature syndrome"
      },
      {
        "code" : "186",
        "display" : "Primary biliary cholangitis"
      },
      {
        "code" : "1860",
        "display" : "Thanatophoric dysplasia type 1"
      },
      {
        "code" : "1861",
        "display" : "Thoracic dysplasia-hydrocephalus syndrome"
      },
      {
        "code" : "1865",
        "display" : "Dyssegmental dysplasia, Silverman-Handmaker type"
      },
      {
        "code" : "1867",
        "display" : "Hereditary bullous dystrophy, macular type"
      },
      {
        "code" : "1871",
        "display" : "Progressive cone dystrophy"
      },
      {
        "code" : "1872",
        "display" : "Cone rod dystrophy"
      },
      {
        "code" : "1873",
        "display" : "Jalili syndrome"
      },
      {
        "code" : "1875",
        "display" : "Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome"
      },
      {
        "code" : "1876",
        "display" : "Oculogastrointestinal muscular dystrophy"
      },
      {
        "code" : "1878",
        "display" : "TRIM32-related limb-girdle muscular dystrophy R8"
      },
      {
        "code" : "1879",
        "display" : "Melorheostosis with osteopoikilosis"
      },
      {
        "code" : "188",
        "display" : "Systemic capillary leak syndrome"
      },
      {
        "code" : "1880",
        "display" : "Ebstein malformation of the tricuspid valve"
      },
      {
        "code" : "1882",
        "display" : "Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome"
      },
      {
        "code" : "1883",
        "display" : "Ectodermal dysplasia-sensorineural deafness syndrome"
      },
      {
        "code" : "1884",
        "display" : "Ectopia lentis-chorioretinal dystrophy-myopia syndrome"
      },
      {
        "code" : "1885",
        "display" : "Isolated ectopia lentis"
      },
      {
        "code" : "189",
        "display" : "Hidrotic ectodermal dysplasia"
      },
      {
        "code" : "1891",
        "display" : "Intellectual disability-spasticity-ectrodactyly syndrome"
      },
      {
        "code" : "1892",
        "display" : "Ectrodactyly-polydactyly syndrome"
      },
      {
        "code" : "189427",
        "display" : "Cushing syndrome due to bilateral macronodular adrenocortical disease"
      },
      {
        "code" : "189466",
        "display" : "Familial isolated hypoparathyroidism due to impaired PTH secretion"
      },
      {
        "code" : "1895",
        "display" : "Edinburgh malformation syndrome"
      },
      {
        "code" : "1896",
        "display" : "EEC syndrome"
      },
      {
        "code" : "1897",
        "display" : "EEM syndrome"
      },
      {
        "code" : "1899",
        "display" : "Arthrochalasia Ehlers-Danlos syndrome"
      },
      {
        "code" : "190",
        "display" : "Coats disease"
      },
      {
        "code" : "1900",
        "display" : "Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency"
      },
      {
        "code" : "1901",
        "display" : "Dermatosparaxis Ehlers-Danlos syndrome"
      },
      {
        "code" : "1902",
        "display" : "Ehrlichiosis"
      },
      {
        "code" : "1906",
        "display" : "Fetal valproate spectrum disorder"
      },
      {
        "code" : "1908",
        "display" : "Aminopterin/methotrexate embryofetopathy"
      },
      {
        "code" : "1909",
        "display" : "Indomethacin embryofetopathy"
      },
      {
        "code" : "191",
        "display" : "Cockayne syndrome"
      },
      {
        "code" : "1910",
        "display" : "Fetal iodine syndrome"
      },
      {
        "code" : "1911",
        "display" : "Cocaine embryofetopathy"
      },
      {
        "code" : "1912",
        "display" : "Fetal hydantoin syndrome"
      },
      {
        "code" : "1913",
        "display" : "Fetal trimethadione syndrome"
      },
      {
        "code" : "1914",
        "display" : "Vitamin K antagonist embryofetopathy"
      },
      {
        "code" : "1915",
        "display" : "Fetal alcohol syndrome"
      },
      {
        "code" : "1916",
        "display" : "Diethylstilbestrol syndrome"
      },
      {
        "code" : "1917",
        "display" : "Fetal methylmercury syndrome"
      },
      {
        "code" : "1918",
        "display" : "Fetal minoxidil syndrome"
      },
      {
        "code" : "1919",
        "display" : "Phenobarbital embryopathy"
      },
      {
        "code" : "192",
        "display" : "Coffin-Lowry syndrome"
      },
      {
        "code" : "1920",
        "display" : "Toluene embryopathy"
      },
      {
        "code" : "1923",
        "display" : "Methimazole embryofetopathy"
      },
      {
        "code" : "1926",
        "display" : "Diabetic embryopathy"
      },
      {
        "code" : "1927",
        "display" : "Emery-Nelson syndrome"
      },
      {
        "code" : "1928",
        "display" : "Congenital lobar emphysema"
      },
      {
        "code" : "1929",
        "display" : "Rasmussen subacute encephalitis"
      },
      {
        "code" : "193",
        "display" : "Cohen syndrome"
      },
      {
        "code" : "1930",
        "display" : "Herpes simplex virus encephalitis"
      },
      {
        "code" : "1931",
        "display" : "Frontal encephalocele"
      },
      {
        "code" : "1933",
        "display" : "Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria"
      },
      {
        "code" : "1934",
        "display" : "Early infantile developmental and epileptic encephalopathy"
      },
      {
        "code" : "1937",
        "display" : "Eng-Strom syndrome"
      },
      {
        "code" : "1941",
        "display" : "Juvenile absence epilepsy"
      },
      {
        "code" : "1942",
        "display" : "Epilepsy with myoclonic-atonic seizures"
      },
      {
        "code" : "1943",
        "display" : "Early-onset progressive encephalopathy with migrant continuous myoclonus"
      },
      {
        "code" : "1945",
        "display" : "Self-limited epilepsy with centrotemporal spikes"
      },
      {
        "code" : "1946",
        "display" : "Amelocerebrohypohidrotic syndrome"
      },
      {
        "code" : "1947",
        "display" : "Northern epilepsy"
      },
      {
        "code" : "1948",
        "display" : "Epilepsy-microcephaly-skeletal dysplasia syndrome"
      },
      {
        "code" : "1949",
        "display" : "Self-limited neonatal epilepsy"
      },
      {
        "code" : "195",
        "display" : "Cat-eye syndrome"
      },
      {
        "code" : "1951",
        "display" : "Epilepsy-telangiectasia syndrome"
      },
      {
        "code" : "1952",
        "display" : "Epiphyseal stippling-osteoclastic hyperplasia syndrome"
      },
      {
        "code" : "1954",
        "display" : "Congenital lethal erythroderma"
      },
      {
        "code" : "1955",
        "display" : "Spinocerebellar ataxia type 34"
      },
      {
        "code" : "1957",
        "display" : "Esthesioneuroblastoma"
      },
      {
        "code" : "1959",
        "display" : "Evans syndrome"
      },
      {
        "code" : "1962",
        "display" : "Exostoses-anetodermia-brachydactyly type E syndrome"
      },
      {
        "code" : "1964",
        "display" : "Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome"
      },
      {
        "code" : "1968",
        "display" : "Flat face-microstomia-ear anomaly syndrome"
      },
      {
        "code" : "1969",
        "display" : "Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome"
      },
      {
        "code" : "1970",
        "display" : "Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome"
      },
      {
        "code" : "1972",
        "display" : "Lethal faciocardiomelic dysplasia"
      },
      {
        "code" : "1973",
        "display" : "Faciocardiorenal syndrome"
      },
      {
        "code" : "1974",
        "display" : "Autosomal recessive faciodigitogenital syndrome"
      },
      {
        "code" : "1979",
        "display" : "Lipodystrophy due to peptidic growth factors deficiency"
      },
      {
        "code" : "198",
        "display" : "Occipital horn syndrome"
      },
      {
        "code" : "1980",
        "display" : "Bilateral striopallidodentate calcinosis"
      },
      {
        "code" : "1986",
        "display" : "Gollop-Wolfgang complex"
      },
      {
        "code" : "1987",
        "display" : "Isolated femoral agenesis/hypoplasia"
      },
      {
        "code" : "1988",
        "display" : "Femoral-facial syndrome"
      },
      {
        "code" : "199",
        "display" : "Cornelia de Lange syndrome"
      },
      {
        "code" : "199241",
        "display" : "Pulmonary capillary hemangiomatosis"
      },
      {
        "code" : "199244",
        "display" : "Nelson syndrome"
      },
      {
        "code" : "199247",
        "display" : "Corticosteroid-binding globulin deficiency"
      },
      {
        "code" : "199251",
        "display" : "Ledderhose disease"
      },
      {
        "code" : "199260",
        "display" : "Calcifying aponeurotic fibroma"
      },
      {
        "code" : "199267",
        "display" : "Infantile digital fibromatosis"
      },
      {
        "code" : "199276",
        "display" : "Familial multiple lipomatosis"
      },
      {
        "code" : "199279",
        "display" : "Familial angiolipomatosis"
      },
      {
        "code" : "199282",
        "display" : "Harlequin syndrome"
      },
      {
        "code" : "199285",
        "display" : "Hereditary hypercarotenemia and vitamin A deficiency"
      },
      {
        "code" : "199293",
        "display" : "Congenital microgastria"
      },
      {
        "code" : "199296",
        "display" : "Congenital isolated ACTH deficiency"
      },
      {
        "code" : "199299",
        "display" : "Late-onset isolated ACTH deficiency"
      },
      {
        "code" : "1993",
        "display" : "Pai syndrome"
      },
      {
        "code" : "199302",
        "display" : "Isolated cleft lip"
      },
      {
        "code" : "199306",
        "display" : "Cleft lip/palate"
      },
      {
        "code" : "199310",
        "display" : "Tetragametic chimerism syndrome"
      },
      {
        "code" : "199315",
        "display" : "Familial clubfoot with or without associated lower limb anomalies"
      },
      {
        "code" : "199318",
        "display" : "15q13.3 microdeletion syndrome"
      },
      {
        "code" : "199323",
        "display" : "Endophthalmitis"
      },
      {
        "code" : "199326",
        "display" : "Isolated autosomal dominant hypomagnesemia, Glaudemans type"
      },
      {
        "code" : "199329",
        "display" : "Congenital myopathy, Paradas type"
      },
      {
        "code" : "199332",
        "display" : "Endocrine-cerebro-osteodysplasia syndrome"
      },
      {
        "code" : "199337",
        "display" : "Pancreatic insufficiency-anemia-hyperostosis syndrome"
      },
      {
        "code" : "199340",
        "display" : "Muscular dystrophy, Selcen type"
      },
      {
        "code" : "199343",
        "display" : "EAST syndrome"
      },
      {
        "code" : "199348",
        "display" : "Thiamine-responsive encephalopathy"
      },
      {
        "code" : "199351",
        "display" : "Adult-onset dystonia-parkinsonism"
      },
      {
        "code" : "199354",
        "display" : "Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy"
      },
      {
        "code" : "1995",
        "display" : "Cleft lip-retinopathy syndrome"
      },
      {
        "code" : "199627",
        "display" : "Atypical autism"
      },
      {
        "code" : "199630",
        "display" : "Isolated cerebellar vermis hypoplasia"
      },
      {
        "code" : "199642",
        "display" : "Isolated congenital microcephaly"
      },
      {
        "code" : "199647",
        "display" : "Isolated encephalocele"
      },
      {
        "code" : "1997",
        "display" : "Blepharo-cheilo-odontic syndrome"
      },
      {
        "code" : "20",
        "display" : "3-hydroxy-3-methylglutaric aciduria"
      },
      {
        "code" : "200",
        "display" : "Isolated corpus callosum agenesis"
      },
      {
        "code" : "2001",
        "display" : "Cleft lip/palate-intestinal malrotation-cardiopathy syndrome"
      },
      {
        "code" : "2003",
        "display" : "Cleft lip/palate-deafness-sacral lipoma syndrome"
      },
      {
        "code" : "2004",
        "display" : "Laryngotracheoesophageal cleft"
      },
      {
        "code" : "200418",
        "display" : "Immunodeficiency with factor I anomaly"
      },
      {
        "code" : "200421",
        "display" : "Immunodeficiency with factor H anomaly"
      },
      {
        "code" : "2006",
        "display" : "Median cleft lip/mandible"
      },
      {
        "code" : "2007",
        "display" : "Alar cartilages hypoplasia-coloboma-telecanthus syndrome"
      },
      {
        "code" : "2008",
        "display" : "Acrocardiofacial syndrome"
      },
      {
        "code" : "201",
        "display" : "Cowden syndrome"
      },
      {
        "code" : "2010",
        "display" : "Cleft palate-stapes fixation-oligodontia syndrome"
      },
      {
        "code" : "2013",
        "display" : "Cleft palate-large ears-small head syndrome"
      },
      {
        "code" : "2015",
        "display" : "Cleft palate-short stature-vertebral anomalies syndrome"
      },
      {
        "code" : "2016",
        "display" : "Cleft palate-lateral synechia syndrome"
      },
      {
        "code" : "2017",
        "display" : "Sternal cleft"
      },
      {
        "code" : "2019",
        "display" : "Femur-fibula-ulna complex"
      },
      {
        "code" : "2020",
        "display" : "Congenital fiber-type disproportion myopathy"
      },
      {
        "code" : "2021",
        "display" : "Fibrochondrogenesis"
      },
      {
        "code" : "2022",
        "display" : "Endocardial fibroelastosis"
      },
      {
        "code" : "2023",
        "display" : "Undifferentiated pleomorphic sarcoma"
      },
      {
        "code" : "2024",
        "display" : "Hereditary gingival fibromatosis"
      },
      {
        "code" : "2025",
        "display" : "Gingival fibromatosis-facial dysmorphism syndrome"
      },
      {
        "code" : "2026",
        "display" : "Gingival fibromatosis-hypertrichosis syndrome"
      },
      {
        "code" : "2027",
        "display" : "Gingival fibromatosis-progressive deafness syndrome"
      },
      {
        "code" : "2028",
        "display" : "Juvenile hyaline fibromatosis"
      },
      {
        "code" : "2030",
        "display" : "Fibrosarcoma"
      },
      {
        "code" : "2031",
        "display" : "Hepatic fibrosis-renal cysts-intellectual disability syndrome"
      },
      {
        "code" : "2032",
        "display" : "Idiopathic pulmonary fibrosis"
      },
      {
        "code" : "2035",
        "display" : "Lymphatic filariasis"
      },
      {
        "code" : "2036",
        "display" : "Scalp-ear-nipple syndrome"
      },
      {
        "code" : "2037",
        "display" : "Congenital aortopulmonary window"
      },
      {
        "code" : "2038",
        "display" : "Pulmonary arteriovenous malformation"
      },
      {
        "code" : "2039",
        "display" : "Congenital systemic arteriovenous fistula"
      },
      {
        "code" : "204",
        "display" : "Sporadic Creutzfeldt-Jakob disease"
      },
      {
        "code" : "2040",
        "display" : "Congenital respiratory-biliary fistula"
      },
      {
        "code" : "2041",
        "display" : "Coronary arterial fistula"
      },
      {
        "code" : "2044",
        "display" : "Floating-Harbor syndrome"
      },
      {
        "code" : "2045",
        "display" : "FLOTCH syndrome"
      },
      {
        "code" : "2047",
        "display" : "Flynn-Aird syndrome"
      },
      {
        "code" : "2048",
        "display" : "Foix-Chavany-Marie syndrome"
      },
      {
        "code" : "205",
        "display" : "Crigler-Najjar syndrome"
      },
      {
        "code" : "2050",
        "display" : "Cole-Carpenter syndrome"
      },
      {
        "code" : "2052",
        "display" : "Fraser syndrome"
      },
      {
        "code" : "2053",
        "display" : "Freeman-Sheldon syndrome"
      },
      {
        "code" : "2056",
        "display" : "Essential fructosuria"
      },
      {
        "code" : "2057",
        "display" : "Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome"
      },
      {
        "code" : "2058",
        "display" : "Fryns-Smeets-Thiry syndrome"
      },
      {
        "code" : "2059",
        "display" : "Fryns syndrome"
      },
      {
        "code" : "2062",
        "display" : "Progressive non-infectious anterior vertebral fusion"
      },
      {
        "code" : "2063",
        "display" : "Splenogonadal fusion-limb defects-micrognathia syndrome"
      },
      {
        "code" : "2064",
        "display" : "Posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome"
      },
      {
        "code" : "206436",
        "display" : "Infantile Krabbe disease"
      },
      {
        "code" : "206443",
        "display" : "Late-infantile/juvenile Krabbe disease"
      },
      {
        "code" : "206448",
        "display" : "Adult Krabbe disease"
      },
      {
        "code" : "206470",
        "display" : "Cystadenoma of childhood"
      },
      {
        "code" : "206484",
        "display" : "Gonadoblastoma"
      },
      {
        "code" : "206489",
        "display" : "Malignant germ cell tumor of the vagina"
      },
      {
        "code" : "206492",
        "display" : "Vulvovaginal rhabdomyosarcoma"
      },
      {
        "code" : "2065",
        "display" : "Galloway-Mowat syndrome"
      },
      {
        "code" : "206538",
        "display" : "Malignant non-dysgerminomatous germ cell tumor of ovary"
      },
      {
        "code" : "206546",
        "display" : "Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers"
      },
      {
        "code" : "206549",
        "display" : "Anoctamin-5-related limb-girdle muscular dystrophy R12"
      },
      {
        "code" : "206554",
        "display" : "Fukutin-related limb-girdle muscular dystrophy R13"
      },
      {
        "code" : "206559",
        "display" : "POMT2-related limb-girdle muscular dystrophy R14"
      },
      {
        "code" : "206564",
        "display" : "POMGNT1-related limb-girdle muscular dystrophy R15"
      },
      {
        "code" : "206569",
        "display" : "Immune-mediated necrotizing myopathy"
      },
      {
        "code" : "206572",
        "display" : "Overlap myositis"
      },
      {
        "code" : "206575",
        "display" : "Rippling muscle disease with myasthenia gravis"
      },
      {
        "code" : "206580",
        "display" : "Autosomal recessive lower motor neuron disease with childhood onset"
      },
      {
        "code" : "206583",
        "display" : "Adult polyglucosan body disease"
      },
      {
        "code" : "206586",
        "display" : "Neurolymphomatosis"
      },
      {
        "code" : "206594",
        "display" : "Subacute inflammatory demyelinating polyneuropathy"
      },
      {
        "code" : "206599",
        "display" : "Isolated asymptomatic elevation of creatine phosphokinase"
      },
      {
        "code" : "2066",
        "display" : "Gamma-aminobutyric acid transaminase deficiency"
      },
      {
        "code" : "2067",
        "display" : "GAPO syndrome"
      },
      {
        "code" : "2069",
        "display" : "Gastrocutaneous syndrome"
      },
      {
        "code" : "206991",
        "display" : "Viral myositis"
      },
      {
        "code" : "206994",
        "display" : "Bacterial myositis"
      },
      {
        "code" : "207",
        "display" : "Crouzon syndrome"
      },
      {
        "code" : "2070",
        "display" : "Eosinophilic gastroenteritis"
      },
      {
        "code" : "207000",
        "display" : "Fungal myositis"
      },
      {
        "code" : "2072",
        "display" : "Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome"
      },
      {
        "code" : "2073",
        "display" : "Narcolepsy type 1"
      },
      {
        "code" : "2074",
        "display" : "Gemignani syndrome"
      },
      {
        "code" : "2075",
        "display" : "Genitopalatocardiac syndrome"
      },
      {
        "code" : "2077",
        "display" : "German syndrome"
      },
      {
        "code" : "2078",
        "display" : "Geroderma osteodysplastica"
      },
      {
        "code" : "2083",
        "display" : "Prominent glabella-microcephaly-hypogenitalism syndrome"
      },
      {
        "code" : "2084",
        "display" : "Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome"
      },
      {
        "code" : "208441",
        "display" : "Bilateral parasagittal parieto-occipital polymicrogyria"
      },
      {
        "code" : "208444",
        "display" : "Bilateral frontal polymicrogyria"
      },
      {
        "code" : "208447",
        "display" : "Bilateral generalized polymicrogyria"
      },
      {
        "code" : "2085",
        "display" : "Glaucoma-sleep apnea syndrome"
      },
      {
        "code" : "208513",
        "display" : "Spinocerebellar ataxia type 29"
      },
      {
        "code" : "208524",
        "display" : "Herpetiform pemphigus"
      },
      {
        "code" : "2086",
        "display" : "Optic pathway glioma"
      },
      {
        "code" : "2088",
        "display" : "Fanconi-Bickel syndrome"
      },
      {
        "code" : "2089",
        "display" : "Glycogen storage disease due to hepatic glycogen synthase deficiency"
      },
      {
        "code" : "208989",
        "display" : "Non-paraneoplastic sensory ganglionopathy"
      },
      {
        "code" : "208999",
        "display" : "Paraneoplastic sensory ganglionopathy"
      },
      {
        "code" : "2090",
        "display" : "GMS syndrome"
      },
      {
        "code" : "209004",
        "display" : "Polyneuropathy associated with IgM monoclonal gammopathy"
      },
      {
        "code" : "2091",
        "display" : "Multinodular goiter-cystic kidney-polydactyly syndrome"
      },
      {
        "code" : "2092",
        "display" : "Focal dermal hypoplasia"
      },
      {
        "code" : "209335",
        "display" : "Autosomal dominant adult-onset proximal spinal muscular atrophy"
      },
      {
        "code" : "209341",
        "display" : "DYNC1H1-related autosomal dominant childhood-onset proximal spinal muscular atrophy"
      },
      {
        "code" : "209370",
        "display" : "MECP2-related severe neonatal encephalopathy"
      },
      {
        "code" : "2095",
        "display" : "Gorlin-Chaudhry-Moss syndrome"
      },
      {
        "code" : "2097",
        "display" : "Grant syndrome"
      },
      {
        "code" : "2098",
        "display" : "Acromesomelic dysplasia, Grebe type"
      },
      {
        "code" : "209867",
        "display" : "Autosomal dominant rhegmatogenous retinal detachment"
      },
      {
        "code" : "209902",
        "display" : "Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency"
      },
      {
        "code" : "209905",
        "display" : "Brain-lung-thyroid syndrome"
      },
      {
        "code" : "209908",
        "display" : "Isolated childhood apraxia of speech"
      },
      {
        "code" : "209916",
        "display" : "Extraskeletal myxoid chondrosarcoma"
      },
      {
        "code" : "209919",
        "display" : "Idiopathic copper-associated cirrhosis"
      },
      {
        "code" : "209932",
        "display" : "Cone dystrophy with supernormal rod response"
      },
      {
        "code" : "209943",
        "display" : "IRVAN syndrome"
      },
      {
        "code" : "209951",
        "display" : "Autosomal spastic paraplegia type 18"
      },
      {
        "code" : "209956",
        "display" : "Idiopathic uveal effusion syndrome"
      },
      {
        "code" : "209959",
        "display" : "Phacoanaphylactic uveitis"
      },
      {
        "code" : "209964",
        "display" : "Solitary rectal ulcer syndrome"
      },
      {
        "code" : "209967",
        "display" : "Episodic ataxia type 6"
      },
      {
        "code" : "209970",
        "display" : "Episodic ataxia type 7"
      },
      {
        "code" : "209973",
        "display" : "Benign nocturnal alternating hemiplegia of childhood"
      },
      {
        "code" : "209981",
        "display" : "IRIDA syndrome"
      },
      {
        "code" : "210",
        "display" : "Cyclosporiasis"
      },
      {
        "code" : "2101",
        "display" : "Grubben-de Cock-Borghgraef syndrome"
      },
      {
        "code" : "210110",
        "display" : "Intermediate osteopetrosis"
      },
      {
        "code" : "210115",
        "display" : "Sterile multifocal osteomyelitis with periostitis and pustulosis"
      },
      {
        "code" : "210122",
        "display" : "Congenital alveolar capillary dysplasia"
      },
      {
        "code" : "210128",
        "display" : "Urocanic aciduria"
      },
      {
        "code" : "210133",
        "display" : "Leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome"
      },
      {
        "code" : "210136",
        "display" : "Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome"
      },
      {
        "code" : "210141",
        "display" : "Inherited congenital spastic tetraplegia"
      },
      {
        "code" : "210144",
        "display" : "Lethal polymalformative syndrome, Boissel type"
      },
      {
        "code" : "210159",
        "display" : "Adult hepatocellular carcinoma"
      },
      {
        "code" : "210163",
        "display" : "Congenital lethal myopathy, Compton-North type"
      },
      {
        "code" : "2102",
        "display" : "GTP cyclohydrolase I deficiency"
      },
      {
        "code" : "210272",
        "display" : "Mal de débarquement"
      },
      {
        "code" : "2104",
        "display" : "Dysmorphism-pectus carinatum-joint laxity syndrome"
      },
      {
        "code" : "210548",
        "display" : "Macrocephaly-intellectual disability-autism syndrome"
      },
      {
        "code" : "210571",
        "display" : "Dystonia 16"
      },
      {
        "code" : "210576",
        "display" : "Congenital temporomandibular joint ankylosis"
      },
      {
        "code" : "210584",
        "display" : "Spindle cell hemangioma"
      },
      {
        "code" : "2107",
        "display" : "Hall-Riggs syndrome"
      },
      {
        "code" : "2108",
        "display" : "Hallermann-Streiff syndrome"
      },
      {
        "code" : "2109",
        "display" : "Hallermann-Streiff-like syndrome"
      },
      {
        "code" : "211",
        "display" : "Familial cylindromatosis"
      },
      {
        "code" : "2110",
        "display" : "Hallux varus-preaxial polysyndactyly syndrome"
      },
      {
        "code" : "211017",
        "display" : "Spinocerebellar ataxia type 30"
      },
      {
        "code" : "211067",
        "display" : "Episodic ataxia type 5"
      },
      {
        "code" : "2111",
        "display" : "Cystic hamartoma of lung and kidney"
      },
      {
        "code" : "2114",
        "display" : "Hip dysplasia, Beukes type"
      },
      {
        "code" : "2115",
        "display" : "Harrod syndrome"
      },
      {
        "code" : "2116",
        "display" : "Hartnup disease"
      },
      {
        "code" : "2117",
        "display" : "Hartsfield syndrome"
      },
      {
        "code" : "2118",
        "display" : "Hawkinsinuria"
      },
      {
        "code" : "2119",
        "display" : "HEC syndrome"
      },
      {
        "code" : "212",
        "display" : "Cystathioninuria"
      },
      {
        "code" : "2122",
        "display" : "Kaposiform hemangioendothelioma"
      },
      {
        "code" : "2123",
        "display" : "Multifocal infantile hemangioma with extracutenous involvement"
      },
      {
        "code" : "2126",
        "display" : "Solitary fibrous tumor"
      },
      {
        "code" : "2128",
        "display" : "Isolated hemihyperplasia"
      },
      {
        "code" : "213",
        "display" : "Cystinosis"
      },
      {
        "code" : "2131",
        "display" : "Alternating hemiplegia of childhood"
      },
      {
        "code" : "2132",
        "display" : "Hemoglobin C disease"
      },
      {
        "code" : "2133",
        "display" : "Hemoglobin E disease"
      },
      {
        "code" : "2134",
        "display" : "Atypical hemolytic uremic syndrome"
      },
      {
        "code" : "2135",
        "display" : "Cutaneous mastocytosis-deafness-microtia syndrome"
      },
      {
        "code" : "213504",
        "display" : "Adenocarcinoma of ovary"
      },
      {
        "code" : "213512",
        "display" : "Malignant mixed Müllerian tumor of the ovary"
      },
      {
        "code" : "213528",
        "display" : "Rare adenocarcinoma of the breast"
      },
      {
        "code" : "213531",
        "display" : "Metaplastic carcinoma of the breast"
      },
      {
        "code" : "213557",
        "display" : "Salivary gland type cancer of the breast"
      },
      {
        "code" : "2136",
        "display" : "Hennekam syndrome"
      },
      {
        "code" : "213600",
        "display" : "Adenosarcoma of the corpus uteri"
      },
      {
        "code" : "213605",
        "display" : "Carcinofibroma of the corpus uteri"
      },
      {
        "code" : "213610",
        "display" : "Carcinosarcoma of the corpus uteri"
      },
      {
        "code" : "213615",
        "display" : "Rhabdomyosarcoma of the corpus uteri"
      },
      {
        "code" : "213625",
        "display" : "Leiomyosarcoma of the corpus uteri"
      },
      {
        "code" : "213630",
        "display" : "Primitive neuroectodermal tumor of the corpus uteri"
      },
      {
        "code" : "2137",
        "display" : "Autoimmune hepatitis"
      },
      {
        "code" : "213711",
        "display" : "Endometrial stromal sarcoma"
      },
      {
        "code" : "213716",
        "display" : "Squamous cell carcinoma of the corpus uteri"
      },
      {
        "code" : "213721",
        "display" : "Undifferentiated carcinoma of the corpus uteri"
      },
      {
        "code" : "213726",
        "display" : "Serous carcinoma of the corpus uteri"
      },
      {
        "code" : "213731",
        "display" : "High-grade neuroendocrine carcinoma of the corpus uteri"
      },
      {
        "code" : "213736",
        "display" : "Low-grade neuroendocrine tumor of the corpus uteri"
      },
      {
        "code" : "213746",
        "display" : "Transitional cell carcinoma of the corpus uteri"
      },
      {
        "code" : "213751",
        "display" : "Malignant germ cell tumor of the corpus uteri"
      },
      {
        "code" : "213767",
        "display" : "Squamous cell carcinoma of the cervix uteri"
      },
      {
        "code" : "213772",
        "display" : "Adenocarcinoma of the cervix uteri"
      },
      {
        "code" : "213777",
        "display" : "High-grade neuroendocrine carcinoma of the cervix uteri"
      },
      {
        "code" : "213787",
        "display" : "Carcinosarcoma of the cervix uteri"
      },
      {
        "code" : "213792",
        "display" : "Adenosarcoma of the cervix uteri"
      },
      {
        "code" : "2138",
        "display" : "46,XX ovotesticular difference of sex development"
      },
      {
        "code" : "213802",
        "display" : "Rhabdomyosarcoma of the cervix uteri"
      },
      {
        "code" : "213807",
        "display" : "Leiomyosarcoma of the cervix uteri"
      },
      {
        "code" : "213812",
        "display" : "Primitive neuroectodermal tumor of the cervix uteri"
      },
      {
        "code" : "213823",
        "display" : "Adenoid cystic carcinoma of the cervix uteri"
      },
      {
        "code" : "213828",
        "display" : "Adenoid basal carcinoma of the cervix uteri"
      },
      {
        "code" : "213833",
        "display" : "Glassy cell carcinoma of the cervix uteri"
      },
      {
        "code" : "213837",
        "display" : "Malignant germ cell tumor of the cervix uteri"
      },
      {
        "code" : "2139",
        "display" : "Hernández-Aguirre Negrete syndrome"
      },
      {
        "code" : "214",
        "display" : "Cystinuria"
      },
      {
        "code" : "2140",
        "display" : "Congenital diaphragmatic hernia"
      },
      {
        "code" : "2141",
        "display" : "Diaphragmatic defect-limb deficiency-skull defect syndrome"
      },
      {
        "code" : "2143",
        "display" : "Donnai-Barrow syndrome"
      },
      {
        "code" : "2145",
        "display" : "Craniosynostosis, Herrmann-Opitz type"
      },
      {
        "code" : "2148",
        "display" : "Lissencephaly type 1 due to doublecortin gene mutation"
      },
      {
        "code" : "2149",
        "display" : "Nodular neuronal heterotopia"
      },
      {
        "code" : "215",
        "display" : "Congenital stationary night blindness"
      },
      {
        "code" : "2150",
        "display" : "Hirschsprung disease-type D brachydactyly syndrome"
      },
      {
        "code" : "2151",
        "display" : "Hirschsprung disease-ganglioneuroblastoma syndrome"
      },
      {
        "code" : "2152",
        "display" : "Mowat-Wilson syndrome"
      },
      {
        "code" : "2153",
        "display" : "Hirschsprung disease-nail hypoplasia-dysmorphism syndrome"
      },
      {
        "code" : "2155",
        "display" : "Hirschsprung disease-deafness-polydactyly syndrome"
      },
      {
        "code" : "2157",
        "display" : "Histidinemia"
      },
      {
        "code" : "2158",
        "display" : "Histidinuria-renal tubular defect syndrome"
      },
      {
        "code" : "2162",
        "display" : "Holoprosencephaly"
      },
      {
        "code" : "2163",
        "display" : "Holoprosencephaly-craniosynostosis syndrome"
      },
      {
        "code" : "2165",
        "display" : "Holoprosencephaly-caudal dysgenesis syndrome"
      },
      {
        "code" : "2166",
        "display" : "Holoprosencephaly-postaxial polydactyly syndrome"
      },
      {
        "code" : "216694",
        "display" : "Congenitally corrected transposition of the great arteries"
      },
      {
        "code" : "2167",
        "display" : "Holzgreve syndrome"
      },
      {
        "code" : "216718",
        "display" : "Isolated congenitally uncorrected transposition of the great arteries"
      },
      {
        "code" : "216729",
        "display" : "Congenitally uncorrected transposition of the great arteries with cardiac malformation"
      },
      {
        "code" : "216796",
        "display" : "Osteogenesis imperfecta type 1"
      },
      {
        "code" : "216804",
        "display" : "Osteogenesis imperfecta type 2"
      },
      {
        "code" : "216812",
        "display" : "Osteogenesis imperfecta type 3"
      },
      {
        "code" : "216820",
        "display" : "Osteogenesis imperfecta type 4"
      },
      {
        "code" : "216828",
        "display" : "Osteogenesis imperfecta type 5"
      },
      {
        "code" : "216866",
        "display" : "Classic pantothenate kinase-associated neurodegeneration"
      },
      {
        "code" : "216873",
        "display" : "Atypical pantothenate kinase-associated neurodegeneration"
      },
      {
        "code" : "2169",
        "display" : "Methylcobalamin deficiency type cblE"
      },
      {
        "code" : "216972",
        "display" : "Niemann-Pick disease type C, severe perinatal form"
      },
      {
        "code" : "216975",
        "display" : "Niemann-Pick disease type C, severe early infantile neurologic onset"
      },
      {
        "code" : "216978",
        "display" : "Niemann-Pick disease type C, late infantile neurologic onset"
      },
      {
        "code" : "216981",
        "display" : "Niemann-Pick disease type C, juvenile neurologic onset"
      },
      {
        "code" : "216986",
        "display" : "Niemann-Pick disease type C, adult neurologic onset"
      },
      {
        "code" : "217",
        "display" : "Isolated Dandy-Walker malformation"
      },
      {
        "code" : "2170",
        "display" : "Methylcobalamin deficiency type cblG"
      },
      {
        "code" : "217008",
        "display" : "Bockenheimer syndrome"
      },
      {
        "code" : "217012",
        "display" : "Spinocerebellar ataxia type 31"
      },
      {
        "code" : "217017",
        "display" : "Zechi-Ceide syndrome"
      },
      {
        "code" : "217026",
        "display" : "Microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type"
      },
      {
        "code" : "217055",
        "display" : "Autosomal recessive intermediate Charcot-Marie-Tooth disease type A"
      },
      {
        "code" : "217059",
        "display" : "Isolated nail clubbing"
      },
      {
        "code" : "217064",
        "display" : "5-fluorouracil poisoning"
      },
      {
        "code" : "217067",
        "display" : "Pouchitis"
      },
      {
        "code" : "217080",
        "display" : "Pulmonary fungal infections in patients deemed at risk"
      },
      {
        "code" : "217085",
        "display" : "Mucopolysaccharidosis type 2, severe form"
      },
      {
        "code" : "217093",
        "display" : "Mucopolysaccharidosis type 2, attenuated form"
      },
      {
        "code" : "2172",
        "display" : "Microcephaly-glomerulonephritis-marfanoid habitus syndrome"
      },
      {
        "code" : "217253",
        "display" : "NMDA receptor encephalitis"
      },
      {
        "code" : "217260",
        "display" : "Progressive multifocal leukoencephalopathy"
      },
      {
        "code" : "217266",
        "display" : "BNAR syndrome"
      },
      {
        "code" : "217330",
        "display" : "REN-related autosomal dominant tubulointerstitial kidney disease"
      },
      {
        "code" : "217335",
        "display" : "RIN2 syndrome"
      },
      {
        "code" : "217340",
        "display" : "17q21.31 microduplication syndrome"
      },
      {
        "code" : "217346",
        "display" : "19q13.11 microdeletion syndrome"
      },
      {
        "code" : "217371",
        "display" : "Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins"
      },
      {
        "code" : "217377",
        "display" : "Microduplication Xp11.22p11.23 syndrome"
      },
      {
        "code" : "217382",
        "display" : "Neurodegenerative syndrome due to cerebral folate transport deficiency"
      },
      {
        "code" : "217385",
        "display" : "17p13.3 microduplication syndrome"
      },
      {
        "code" : "217390",
        "display" : "Combined immunodeficiency due to DOCK8 deficiency"
      },
      {
        "code" : "217396",
        "display" : "Progressive polyneuropathy with bilateral striatal necrosis"
      },
      {
        "code" : "217399",
        "display" : "Congenital insensitivity to pain-hyperhidrosis-absence of cutaneous sensory innervation"
      },
      {
        "code" : "217407",
        "display" : "Hereditary hypotrichosis with recurrent skin vesicles"
      },
      {
        "code" : "217467",
        "display" : "Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency"
      },
      {
        "code" : "217557",
        "display" : "Pulmonary interstitial glycogenosis"
      },
      {
        "code" : "217560",
        "display" : "Neuroendocrine cell hyperplasia of infancy"
      },
      {
        "code" : "217563",
        "display" : "Neonatal acute respiratory distress syndrome"
      },
      {
        "code" : "217566",
        "display" : "Chronic respiratory distress with surfactant metabolism deficiency"
      },
      {
        "code" : "2176",
        "display" : "Infantile systemic hyalinosis"
      },
      {
        "code" : "217622",
        "display" : "Sensorineural deafness with dilated cardiomyopathy"
      },
      {
        "code" : "217656",
        "display" : "Inherited isolated arrhythmogenic cardiomyopathy"
      },
      {
        "code" : "2177",
        "display" : "Hydranencephaly"
      },
      {
        "code" : "218",
        "display" : "Darier disease"
      },
      {
        "code" : "2180",
        "display" : "Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome"
      },
      {
        "code" : "2181",
        "display" : "Hydrocephaly-tall stature-joint laxity syndrome"
      },
      {
        "code" : "2182",
        "display" : "Hydrocephalus with stenosis of the aqueduct of Sylvius"
      },
      {
        "code" : "2183",
        "display" : "Hydrocephalus-obesity-hypogonadism syndrome"
      },
      {
        "code" : "2184",
        "display" : "Hydrocephaly-low insertion umbilicus syndrome"
      },
      {
        "code" : "2185",
        "display" : "Congenital hydrocephalus"
      },
      {
        "code" : "2186",
        "display" : "Hydrocephalus-blue sclerae-nephropathy syndrome"
      },
      {
        "code" : "2189",
        "display" : "Hydrolethalus"
      },
      {
        "code" : "219",
        "display" : "Delta-sarcoglycan-related limb-girdle muscular dystrophy R6"
      },
      {
        "code" : "2195",
        "display" : "Dicarboxylic aminoaciduria"
      },
      {
        "code" : "2196",
        "display" : "Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement"
      },
      {
        "code" : "2197",
        "display" : "Idiopathic hypercalciuria"
      },
      {
        "code" : "2198",
        "display" : "Palmoplantar keratoderma-esophageal carcinoma syndrome"
      },
      {
        "code" : "2199",
        "display" : "Epidermolytic palmoplantar keratoderma"
      },
      {
        "code" : "22",
        "display" : "Succinic semialdehyde dehydrogenase deficiency"
      },
      {
        "code" : "220",
        "display" : "Denys-Drash syndrome"
      },
      {
        "code" : "2200",
        "display" : "Focal palmoplantar and gingival keratoderma"
      },
      {
        "code" : "2201",
        "display" : "Palmoplantar keratoderma-spastic paralysis syndrome"
      },
      {
        "code" : "2202",
        "display" : "Palmoplantar keratoderma-deafness syndrome"
      },
      {
        "code" : "220295",
        "display" : "Xeroderma pigmentosum-Cockayne syndrome complex"
      },
      {
        "code" : "2203",
        "display" : "Hyperlysinemia"
      },
      {
        "code" : "220386",
        "display" : "Semilobar holoprosencephaly"
      },
      {
        "code" : "220393",
        "display" : "Diffuse cutaneous systemic sclerosis"
      },
      {
        "code" : "2204",
        "display" : "Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type"
      },
      {
        "code" : "220402",
        "display" : "Limited cutaneous systemic sclerosis"
      },
      {
        "code" : "220407",
        "display" : "Limited systemic sclerosis"
      },
      {
        "code" : "220436",
        "display" : "Quebec platelet disorder"
      },
      {
        "code" : "220443",
        "display" : "Bleeding diathesis due to thromboxane synthesis deficiency"
      },
      {
        "code" : "220448",
        "display" : "Macrothrombocytopenia with mitral valve insufficiency"
      },
      {
        "code" : "220460",
        "display" : "Attenuated familial adenomatous polyposis"
      },
      {
        "code" : "220465",
        "display" : "Laron syndrome with immunodeficiency"
      },
      {
        "code" : "220493",
        "display" : "Joubert syndrome with ocular defect"
      },
      {
        "code" : "220497",
        "display" : "Joubert syndrome with renal defect"
      },
      {
        "code" : "2206",
        "display" : "Ankylosing vertebral hyperostosis with tylosis"
      },
      {
        "code" : "2209",
        "display" : "Maternal phenylketonuria syndrome"
      },
      {
        "code" : "221",
        "display" : "Dermatomyositis"
      },
      {
        "code" : "221008",
        "display" : "Rothmund-Thomson syndrome type 1"
      },
      {
        "code" : "221016",
        "display" : "Rothmund-Thomson syndrome type 2"
      },
      {
        "code" : "221039",
        "display" : "Hereditary sclerosing poikiloderma, Weary type"
      },
      {
        "code" : "221043",
        "display" : "Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome"
      },
      {
        "code" : "221046",
        "display" : "Poikiloderma with neutropenia"
      },
      {
        "code" : "221054",
        "display" : "Acrocephalopolydactyly"
      },
      {
        "code" : "221061",
        "display" : "Familial cerebral cavernous malformation"
      },
      {
        "code" : "221074",
        "display" : "Marchiafava-Bignami disease"
      },
      {
        "code" : "221078",
        "display" : "Combined hyperactive dysfunction syndrome of the cranial nerves"
      },
      {
        "code" : "221083",
        "display" : "Hemifacial spasm"
      },
      {
        "code" : "221091",
        "display" : "Trigeminal neuralgia"
      },
      {
        "code" : "221098",
        "display" : "Glossopharyngeal neuralgia"
      },
      {
        "code" : "2211",
        "display" : "Hypertelorism-hypospadias-polysyndactyly syndrome"
      },
      {
        "code" : "221117",
        "display" : "Gerstmann syndrome"
      },
      {
        "code" : "221120",
        "display" : "Pseudoaminopterin syndrome"
      },
      {
        "code" : "221126",
        "display" : "Fowler vasculopathy"
      },
      {
        "code" : "221139",
        "display" : "Combined immunodeficiency with facio-oculo-skeletal anomalies"
      },
      {
        "code" : "221142",
        "display" : "Confetti-like macular atrophy"
      },
      {
        "code" : "221145",
        "display" : "Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies"
      },
      {
        "code" : "2213",
        "display" : "Hypertelorism-microtia-facial clefting syndrome"
      },
      {
        "code" : "2215",
        "display" : "Multiple pterygium-malignant hyperthermia syndrome"
      },
      {
        "code" : "2216",
        "display" : "Maternal hyperthermia-induced birth defects"
      },
      {
        "code" : "2218",
        "display" : "Cervical hypertrichosis-peripheral neuropathy syndrome"
      },
      {
        "code" : "222",
        "display" : "Erosive pustular dermatosis of the scalp"
      },
      {
        "code" : "2220",
        "display" : "Hypertrichosis cubiti"
      },
      {
        "code" : "2221",
        "display" : "Acquired hypertrichosis lanuginosa"
      },
      {
        "code" : "2222",
        "display" : "Hypertrichosis lanuginosa congenita"
      },
      {
        "code" : "2224",
        "display" : "Hypertryptophanemia"
      },
      {
        "code" : "2228",
        "display" : "Hypodontia-dysplasia of nails syndrome"
      },
      {
        "code" : "2229",
        "display" : "Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome"
      },
      {
        "code" : "223",
        "display" : "Arginine vasopressin resistance"
      },
      {
        "code" : "2230",
        "display" : "Hypogonadotropic hypogonadism-frontoparietal alopecia syndrome"
      },
      {
        "code" : "2232",
        "display" : "Primary hypergonadotropic hypogonadism-partial alopecia syndrome"
      },
      {
        "code" : "2233",
        "display" : "Hypogonadism-mitral valve prolapse-intellectual disability syndrome"
      },
      {
        "code" : "2234",
        "display" : "Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome"
      },
      {
        "code" : "2235",
        "display" : "Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome"
      },
      {
        "code" : "2237",
        "display" : "Hypoparathyroidism-sensorineural deafness-renal disease syndrome"
      },
      {
        "code" : "2238",
        "display" : "Familial isolated hypoparathyroidism"
      },
      {
        "code" : "2239",
        "display" : "Familial isolated hypoparathyroidism due to agenesis of parathyroid gland"
      },
      {
        "code" : "2241",
        "display" : "Megacystis-microcolon-intestinal hypoperistalsis syndrome"
      },
      {
        "code" : "2246",
        "display" : "Cerebellar hypoplasia-tapetoretinal degeneration syndrome"
      },
      {
        "code" : "2248",
        "display" : "Hypoplastic left heart syndrome"
      },
      {
        "code" : "2249",
        "display" : "Ulna hypoplasia-intellectual disability syndrome"
      },
      {
        "code" : "2250",
        "display" : "Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome"
      },
      {
        "code" : "2251",
        "display" : "Thumb deformity-alopecia-pigmentation anomaly syndrome"
      },
      {
        "code" : "225123",
        "display" : "TFR2-related hemochromatosis"
      },
      {
        "code" : "225147",
        "display" : "Sporadic infantile bilateral striatal necrosis"
      },
      {
        "code" : "225154",
        "display" : "Familial infantile bilateral striatal necrosis"
      },
      {
        "code" : "2252",
        "display" : "Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome"
      },
      {
        "code" : "2253",
        "display" : "Foveal hypoplasia-presenile cataract syndrome"
      },
      {
        "code" : "2254",
        "display" : "Pontocerebellar hypoplasia type 1"
      },
      {
        "code" : "2255",
        "display" : "Pancreatic hypoplasia-diabetes-congenital heart disease syndrome"
      },
      {
        "code" : "2256",
        "display" : "Fibulo-ulnar hypoplasia-renal anomalies syndrome"
      },
      {
        "code" : "2257",
        "display" : "Primary pulmonary hypoplasia"
      },
      {
        "code" : "226",
        "display" : "Dihydropteridine reductase deficiency"
      },
      {
        "code" : "2260",
        "display" : "Oligomeganephronia"
      },
      {
        "code" : "2261",
        "display" : "Hypospadias-intellectual disability, Goldblatt type syndrome"
      },
      {
        "code" : "226307",
        "display" : "Hypothyroidism due to deficient transcription factors involved in pituitary development or function"
      },
      {
        "code" : "226313",
        "display" : "Congenital hypothyroidism due to maternal intake of antithyroid drugs"
      },
      {
        "code" : "226316",
        "display" : "Genetic transient congenital hypothyroidism"
      },
      {
        "code" : "2266",
        "display" : "Hypotrichosis-intellectual disability, Lopes type"
      },
      {
        "code" : "2268",
        "display" : "ICF syndrome"
      },
      {
        "code" : "2269",
        "display" : "Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome"
      },
      {
        "code" : "227",
        "display" : "Diphallia"
      },
      {
        "code" : "2271",
        "display" : "Congenital ichthyosis-microcephalus-tetraplegia syndrome"
      },
      {
        "code" : "2272",
        "display" : "Ichthyosis-oral and digital anomalies syndrome"
      },
      {
        "code" : "2273",
        "display" : "Ichthyosis follicularis-alopecia-photophobia syndrome"
      },
      {
        "code" : "2274",
        "display" : "Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome"
      },
      {
        "code" : "227510",
        "display" : "Multiple system atrophy, cerebellar type"
      },
      {
        "code" : "227535",
        "display" : "Hereditary breast cancer"
      },
      {
        "code" : "227796",
        "display" : "Fundus albipunctatus"
      },
      {
        "code" : "2278",
        "display" : "Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome"
      },
      {
        "code" : "227972",
        "display" : "Toxic oil syndrome"
      },
      {
        "code" : "227976",
        "display" : "Autosomal recessive optic atrophy, OPA7 type"
      },
      {
        "code" : "227982",
        "display" : "Autoimmune polyendocrinopathy type 3"
      },
      {
        "code" : "227990",
        "display" : "Autoimmune polyendocrinopathy type 4"
      },
      {
        "code" : "228000",
        "display" : "Idiopathic CD4 lymphocytopenia"
      },
      {
        "code" : "228003",
        "display" : "Severe combined immunodeficiency due to CORO1A deficiency"
      },
      {
        "code" : "228012",
        "display" : "Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome"
      },
      {
        "code" : "228113",
        "display" : "Anal fistula"
      },
      {
        "code" : "228116",
        "display" : "Hughes-Stovin syndrome"
      },
      {
        "code" : "228119",
        "display" : "Fusariosis"
      },
      {
        "code" : "228123",
        "display" : "Coccidioidomycosis"
      },
      {
        "code" : "228140",
        "display" : "Idiopathic ventricular fibrillation"
      },
      {
        "code" : "228157",
        "display" : "Marburg acute multiple sclerosis"
      },
      {
        "code" : "228165",
        "display" : "Baló concentric sclerosis"
      },
      {
        "code" : "228169",
        "display" : "Autosomal dominant striatal neurodegeneration"
      },
      {
        "code" : "228174",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2N"
      },
      {
        "code" : "228179",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2M"
      },
      {
        "code" : "228190",
        "display" : "Patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome"
      },
      {
        "code" : "2282",
        "display" : "Dysmorphism-short stature-deafness-difference of sex development syndrome"
      },
      {
        "code" : "228227",
        "display" : "Late-onset focal dermal elastosis"
      },
      {
        "code" : "228236",
        "display" : "Linear focal elastosis"
      },
      {
        "code" : "228240",
        "display" : "Elastoderma"
      },
      {
        "code" : "228243",
        "display" : "Elastofibroma dorsi"
      },
      {
        "code" : "228247",
        "display" : "Acquired pseudoxanthoma elasticum"
      },
      {
        "code" : "228254",
        "display" : "Elastoma"
      },
      {
        "code" : "228264",
        "display" : "Papular elastorrhexis"
      },
      {
        "code" : "228272",
        "display" : "Primary anetoderma"
      },
      {
        "code" : "228277",
        "display" : "Familial anetoderma"
      },
      {
        "code" : "228285",
        "display" : "Acquired cutis laxa"
      },
      {
        "code" : "228290",
        "display" : "White fibrous papulosis of the neck"
      },
      {
        "code" : "228293",
        "display" : "Pseudoxanthoma elasticum-like papillary dermal elastolysis"
      },
      {
        "code" : "228299",
        "display" : "Mid-dermal elastolysis"
      },
      {
        "code" : "228302",
        "display" : "Carnitine palmitoyl transferase II deficiency, myopathic form"
      },
      {
        "code" : "228305",
        "display" : "Carnitine palmitoyl transferase II deficiency, severe infantile form"
      },
      {
        "code" : "228308",
        "display" : "Carnitine palmitoyl transferase II deficiency, neonatal form"
      },
      {
        "code" : "228329",
        "display" : "CLN1 disease"
      },
      {
        "code" : "228337",
        "display" : "CLN10 disease"
      },
      {
        "code" : "228343",
        "display" : "CLN4 disease"
      },
      {
        "code" : "228346",
        "display" : "CLN3 disease"
      },
      {
        "code" : "228349",
        "display" : "CLN2 disease"
      },
      {
        "code" : "228354",
        "display" : "CLN8 disease"
      },
      {
        "code" : "228360",
        "display" : "CLN5 disease"
      },
      {
        "code" : "228363",
        "display" : "CLN6 disease"
      },
      {
        "code" : "228366",
        "display" : "CLN7 disease"
      },
      {
        "code" : "228371",
        "display" : "Foodborne botulism"
      },
      {
        "code" : "228374",
        "display" : "Charcot-Marie-Tooth disease type 2B5"
      },
      {
        "code" : "228379",
        "display" : "Virus-associated trichodysplasia spinulosa"
      },
      {
        "code" : "228384",
        "display" : "5q14.3 microdeletion syndrome"
      },
      {
        "code" : "228387",
        "display" : "Spondylo-megaepiphyseal-metaphyseal dysplasia"
      },
      {
        "code" : "228390",
        "display" : "Frontonasal dysplasia-alopecia-genital anomalies syndrome"
      },
      {
        "code" : "228396",
        "display" : "Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome"
      },
      {
        "code" : "228399",
        "display" : "8q12 microduplication syndrome"
      },
      {
        "code" : "228402",
        "display" : "2q23.1 microdeletion syndrome"
      },
      {
        "code" : "228410",
        "display" : "Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome"
      },
      {
        "code" : "228415",
        "display" : "5q35 microduplication syndrome"
      },
      {
        "code" : "228423",
        "display" : "GATA2 deficiency spectrum"
      },
      {
        "code" : "228426",
        "display" : "Syndromic multisystem autoimmune disease due to Itch deficiency"
      },
      {
        "code" : "228429",
        "display" : "Congenital generalized  lipodystrophy type 4"
      },
      {
        "code" : "2285",
        "display" : "Primary basilar invagination"
      },
      {
        "code" : "2287",
        "display" : "Fused mandibular incisors"
      },
      {
        "code" : "2289",
        "display" : "Neuronal intranuclear inclusion disease"
      },
      {
        "code" : "229",
        "display" : "Familial aortic dissection"
      },
      {
        "code" : "2290",
        "display" : "Microvillus inclusion disease"
      },
      {
        "code" : "2291",
        "display" : "Congenital velopharyngeal incompetence"
      },
      {
        "code" : "2295",
        "display" : "Familial articular hypermobility syndrome"
      },
      {
        "code" : "2297",
        "display" : "Insulin-resistance syndrome type A"
      },
      {
        "code" : "229717",
        "display" : "Non-syndromic agammaglobulinemia"
      },
      {
        "code" : "2298",
        "display" : "Insulin-resistance syndrome type B"
      },
      {
        "code" : "2299",
        "display" : "Aortic arch interruption"
      },
      {
        "code" : "23",
        "display" : "Argininosuccinic aciduria"
      },
      {
        "code" : "230",
        "display" : "Dopamine beta-hydroxylase deficiency"
      },
      {
        "code" : "2300",
        "display" : "Isolated multiple intestinal atresia"
      },
      {
        "code" : "2301",
        "display" : "Congenital short bowel syndrome"
      },
      {
        "code" : "2302",
        "display" : "Asbestos intoxication"
      },
      {
        "code" : "2305",
        "display" : "Isotretinoin syndrome"
      },
      {
        "code" : "2306",
        "display" : "Isotretinoin-like syndrome"
      },
      {
        "code" : "2307",
        "display" : "IVIC syndrome"
      },
      {
        "code" : "2308",
        "display" : "Jacobsen syndrome"
      },
      {
        "code" : "230800",
        "display" : "Toxin-mediated infectious botulism"
      },
      {
        "code" : "230839",
        "display" : "Classical-like Ehlers-Danlos syndrome type 1"
      },
      {
        "code" : "230851",
        "display" : "Cardiac-valvular Ehlers-Danlos syndrome"
      },
      {
        "code" : "230857",
        "display" : "Ehlers-Danlos/osteogenesis imperfecta syndrome"
      },
      {
        "code" : "2309",
        "display" : "Pachyonychia congenita"
      },
      {
        "code" : "231",
        "display" : "Dracunculiasis"
      },
      {
        "code" : "2310",
        "display" : "Absence deformity of leg-cataract syndrome"
      },
      {
        "code" : "231013",
        "display" : "Congenital trigeminal anesthesia"
      },
      {
        "code" : "231031",
        "display" : "Erythema palmare hereditarium"
      },
      {
        "code" : "231040",
        "display" : "Familial generalized lentiginosis"
      },
      {
        "code" : "231080",
        "display" : "High-grade dysplasia in patients with Barrett esophagus"
      },
      {
        "code" : "2311",
        "display" : "Autosomal recessive spondylocostal dysostosis"
      },
      {
        "code" : "231108",
        "display" : "Rhabdoid tumor predisposition syndrome"
      },
      {
        "code" : "231111",
        "display" : "Drug-induced lupus erythematosus"
      },
      {
        "code" : "231117",
        "display" : "Beckwith-Wiedemann syndrome due to imprinting defect of 11p15"
      },
      {
        "code" : "231120",
        "display" : "Beckwith-Wiedemann syndrome due to CDKN1C mutation"
      },
      {
        "code" : "231127",
        "display" : "Beckwith-Wiedemann syndrome due to 11p15 microdeletion"
      },
      {
        "code" : "231130",
        "display" : "Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion"
      },
      {
        "code" : "231137",
        "display" : "Silver-Russell syndrome due to 7p11.2p13 microduplication"
      },
      {
        "code" : "231140",
        "display" : "Silver-Russell syndrome due to an imprinting defect of 11p15"
      },
      {
        "code" : "231144",
        "display" : "Silver-Russell syndrome due to 11p15 microduplication"
      },
      {
        "code" : "231147",
        "display" : "Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11"
      },
      {
        "code" : "231154",
        "display" : "Combined immunodeficiency due to partial RAG1 deficiency"
      },
      {
        "code" : "231160",
        "display" : "Familial cerebral saccular aneurysm"
      },
      {
        "code" : "231169",
        "display" : "Usher syndrome type 1"
      },
      {
        "code" : "231178",
        "display" : "Usher syndrome type 2"
      },
      {
        "code" : "231183",
        "display" : "Usher syndrome type 3"
      },
      {
        "code" : "2312",
        "display" : "Transient familial neonatal hyperbilirubinemia"
      },
      {
        "code" : "231205",
        "display" : "Common variable immunodeficiency without known genetic defect"
      },
      {
        "code" : "231214",
        "display" : "Beta-thalassemia major"
      },
      {
        "code" : "231222",
        "display" : "Beta-thalassemia intermedia"
      },
      {
        "code" : "231226",
        "display" : "Dominant beta-thalassemia"
      },
      {
        "code" : "231237",
        "display" : "Delta-beta-thalassemia"
      },
      {
        "code" : "231242",
        "display" : "Hemoglobin C-beta-thalassemia syndrome"
      },
      {
        "code" : "231249",
        "display" : "Hemoglobin E-beta-thalassemia syndrome"
      },
      {
        "code" : "231393",
        "display" : "Beta-thalassemia-X-linked thrombocytopenia syndrome"
      },
      {
        "code" : "2314",
        "display" : "Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency"
      },
      {
        "code" : "231401",
        "display" : "Alpha-thalassemia-myelodysplastic syndrome"
      },
      {
        "code" : "231426",
        "display" : "Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome"
      },
      {
        "code" : "231445",
        "display" : "Paraparetic variant of Guillain-Barré syndrome"
      },
      {
        "code" : "231450",
        "display" : "Acute pure sensory neuropathy"
      },
      {
        "code" : "231457",
        "display" : "Acute pandysautonomia"
      },
      {
        "code" : "231466",
        "display" : "Acute sensory ataxic neuropathy"
      },
      {
        "code" : "2315",
        "display" : "Johanson-Blizzard syndrome"
      },
      {
        "code" : "231500",
        "display" : "Hermansky-Pudlak syndrome due to BLOC-3 deficiency"
      },
      {
        "code" : "231512",
        "display" : "Hermansky-Pudlak syndrome due to BLOC-2 deficiency"
      },
      {
        "code" : "231531",
        "display" : "Hermansky-Pudlak syndrome due to BLOC-1 deficiency"
      },
      {
        "code" : "231556",
        "display" : "Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome"
      },
      {
        "code" : "231568",
        "display" : "Autosomal dominant generalized dystrophic epidermolysis bullosa"
      },
      {
        "code" : "231573",
        "display" : "Congenital erosive and vesicular dermatosis"
      },
      {
        "code" : "231580",
        "display" : "Primary unilateral adrenal hyperplasia"
      },
      {
        "code" : "2316",
        "display" : "Johnson neuroectodermal syndrome"
      },
      {
        "code" : "231625",
        "display" : "Adrenocortical carcinoma with pure aldosterone hypersecretion"
      },
      {
        "code" : "231632",
        "display" : "Ectopic aldosterone-producing tumor"
      },
      {
        "code" : "231662",
        "display" : "Isolated growth hormone deficiency type IA"
      },
      {
        "code" : "231671",
        "display" : "Isolated growth hormone deficiency type IB"
      },
      {
        "code" : "231679",
        "display" : "Isolated growth hormone deficiency type II"
      },
      {
        "code" : "231692",
        "display" : "Isolated growth hormone deficiency type III"
      },
      {
        "code" : "231720",
        "display" : "Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome"
      },
      {
        "code" : "231736",
        "display" : "Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome"
      },
      {
        "code" : "231742",
        "display" : "Epibulbar lipodermoid-preauricular appendage-polythelia syndrome"
      },
      {
        "code" : "2318",
        "display" : "Joubert syndrome with oculorenal defect"
      },
      {
        "code" : "2319",
        "display" : "Juberg-Hayward syndrome"
      },
      {
        "code" : "232",
        "display" : "Sickle cell anemia"
      },
      {
        "code" : "2321",
        "display" : "Jung syndrome"
      },
      {
        "code" : "2322",
        "display" : "Kabuki syndrome"
      },
      {
        "code" : "2323",
        "display" : "Sanjad-Sakati syndrome"
      },
      {
        "code" : "2324",
        "display" : "Osteopenia-intellectual disability-sparse hair syndrome"
      },
      {
        "code" : "2325",
        "display" : "Epidermolysis bullosa simplex with anodontia/hypodontia"
      },
      {
        "code" : "2326",
        "display" : "Kallmann syndrome-heart disease syndrome"
      },
      {
        "code" : "2328",
        "display" : "Kapur-Toriello syndrome"
      },
      {
        "code" : "2329",
        "display" : "Karsch-Neugebauer syndrome"
      },
      {
        "code" : "233",
        "display" : "Duane retraction syndrome"
      },
      {
        "code" : "2330",
        "display" : "Kasabach-Merritt phenomenon"
      },
      {
        "code" : "2331",
        "display" : "Kawasaki disease"
      },
      {
        "code" : "2332",
        "display" : "KBG syndrome"
      },
      {
        "code" : "2333",
        "display" : "Kenny-Caffey syndrome"
      },
      {
        "code" : "2334",
        "display" : "Autosomal dominant keratitis"
      },
      {
        "code" : "2337",
        "display" : "Diffuse palmoplantar keratoderma, Bothnian type"
      },
      {
        "code" : "2339",
        "display" : "Keratosis follicularis-dwarfism-cerebral atrophy syndrome"
      },
      {
        "code" : "234",
        "display" : "Dubin-Johnson syndrome"
      },
      {
        "code" : "2340",
        "display" : "Keratosis follicularis spinulosa decalvans"
      },
      {
        "code" : "2342",
        "display" : "Haim-Munk syndrome"
      },
      {
        "code" : "2345",
        "display" : "Isolated Klippel-Feil syndrome"
      },
      {
        "code" : "2347",
        "display" : "Lethal Kniest-like dysplasia"
      },
      {
        "code" : "2348",
        "display" : "Familial partial lipodystrophy, Dunnigan type"
      },
      {
        "code" : "2349",
        "display" : "Muscular pseudohypertrophy-hypothyroidism syndrome"
      },
      {
        "code" : "235",
        "display" : "Dubowitz syndrome"
      },
      {
        "code" : "2351",
        "display" : "Kousseff syndrome"
      },
      {
        "code" : "2353",
        "display" : "Schilbach-Rott syndrome"
      },
      {
        "code" : "2356",
        "display" : "Arachnoid cyst"
      },
      {
        "code" : "2357",
        "display" : "Bronchogenic cyst"
      },
      {
        "code" : "236",
        "display" : "Trisomy 9p syndrome"
      },
      {
        "code" : "2363",
        "display" : "Lacrimoauriculodentodigital syndrome"
      },
      {
        "code" : "2364",
        "display" : "Glycogen storage disease due to lactate dehydrogenase deficiency"
      },
      {
        "code" : "2368",
        "display" : "Gastroschisis"
      },
      {
        "code" : "2369",
        "display" : "Limb body wall complex"
      },
      {
        "code" : "237",
        "display" : "Duplication of urethra"
      },
      {
        "code" : "2370",
        "display" : "Larsen-like osseous dysplasia-short stature syndrome"
      },
      {
        "code" : "2371",
        "display" : "Lethal Larsen-like syndrome"
      },
      {
        "code" : "2372",
        "display" : "Laryngocele"
      },
      {
        "code" : "2373",
        "display" : "Congenital laryngomalacia"
      },
      {
        "code" : "2374",
        "display" : "Isolated congenital laryngeal web"
      },
      {
        "code" : "2375",
        "display" : "Laryngeal abductor paralysis-intellectual disability syndrome"
      },
      {
        "code" : "2377",
        "display" : "Laurence-Moon syndrome"
      },
      {
        "code" : "2378",
        "display" : "Laurin-Sandrow syndrome"
      },
      {
        "code" : "2379",
        "display" : "Early-onset parkinsonism-intellectual disability syndrome"
      },
      {
        "code" : "2380",
        "display" : "Legg-Calvé-Perthes disease"
      },
      {
        "code" : "2382",
        "display" : "Lennox-Gastaut syndrome"
      },
      {
        "code" : "238269",
        "display" : "AApoAII amyloidosis"
      },
      {
        "code" : "238305",
        "display" : "Infundibulo-neurohypophysitis"
      },
      {
        "code" : "238329",
        "display" : "Severe X-linked mitochondrial encephalomyopathy"
      },
      {
        "code" : "238446",
        "display" : "15q11q13 microduplication syndrome"
      },
      {
        "code" : "238455",
        "display" : "Infantile dystonia-parkinsonism"
      },
      {
        "code" : "238459",
        "display" : "SLC35A1-CDG"
      },
      {
        "code" : "238468",
        "display" : "Hypohidrotic ectodermal dysplasia"
      },
      {
        "code" : "238475",
        "display" : "Familial hypercholanemia"
      },
      {
        "code" : "238505",
        "display" : "Combined immunodeficiency due to CD27 deficiency"
      },
      {
        "code" : "238523",
        "display" : "Atypical hypotonia-cystinuria syndrome"
      },
      {
        "code" : "238557",
        "display" : "Chuvash erythrocytosis"
      },
      {
        "code" : "238569",
        "display" : "Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome"
      },
      {
        "code" : "238578",
        "display" : "Familial clubfoot due to 17q23.1q23.2 microduplication"
      },
      {
        "code" : "238583",
        "display" : "Hyperphenylalaninemia due to tetrahydrobiopterin deficiency"
      },
      {
        "code" : "238593",
        "display" : "IgG4-related mesenteritis"
      },
      {
        "code" : "2386",
        "display" : "Leukoencephalopathy-palmoplantar keratoderma syndrome"
      },
      {
        "code" : "238606",
        "display" : "Primary orthostatic tremor"
      },
      {
        "code" : "238613",
        "display" : "Beckwith-Wiedemann syndrome due to NSD1 mutation"
      },
      {
        "code" : "238621",
        "display" : "Ileal pouch anal anastomosis related faecal incontinence"
      },
      {
        "code" : "238624",
        "display" : "Idiopathic intracranial hypertension"
      },
      {
        "code" : "238637",
        "display" : "Megacystis-megaureter syndrome"
      },
      {
        "code" : "238642",
        "display" : "Primary megaureter, adult-onset form"
      },
      {
        "code" : "238646",
        "display" : "Congenital primary megaureter, obstructed form"
      },
      {
        "code" : "238650",
        "display" : "Congenital primary megaureter, refluxing form"
      },
      {
        "code" : "238654",
        "display" : "Congenital primary megaureter, nonrefluxing and unobstructed form"
      },
      {
        "code" : "238666",
        "display" : "Isolated congenital hypogonadotropic hypogonadism"
      },
      {
        "code" : "238670",
        "display" : "Isolated thyrotropin-releasing hormone deficiency"
      },
      {
        "code" : "238688",
        "display" : "Neonatal iodine exposure"
      },
      {
        "code" : "2387",
        "display" : "Leukonychia totalis"
      },
      {
        "code" : "238722",
        "display" : "Familial congenital mirror movements"
      },
      {
        "code" : "238744",
        "display" : "Mammary-digital-nail syndrome"
      },
      {
        "code" : "238750",
        "display" : "4q21 microdeletion syndrome"
      },
      {
        "code" : "238763",
        "display" : "Glaucoma secondary to spherophakia/ectopia lentis and megalocornea"
      },
      {
        "code" : "238769",
        "display" : "1q44 microdeletion syndrome"
      },
      {
        "code" : "2388",
        "display" : "Choreoacanthocytosis"
      },
      {
        "code" : "239",
        "display" : "Dyggve-Melchior-Clausen disease"
      },
      {
        "code" : "2390",
        "display" : "Lichtenstein syndrome"
      },
      {
        "code" : "2391",
        "display" : "Congenitally short costocoracoid ligament"
      },
      {
        "code" : "2394",
        "display" : "Pyruvate dehydrogenase E3 deficiency"
      },
      {
        "code" : "2396",
        "display" : "Encephalocraniocutaneous lipomatosis"
      },
      {
        "code" : "2398",
        "display" : "Multiple symmetric lipomatosis"
      },
      {
        "code" : "2399",
        "display" : "Nasopalpebral lipoma-coloboma syndrome"
      },
      {
        "code" : "24",
        "display" : "Fumaric aciduria"
      },
      {
        "code" : "240",
        "display" : "Léri-Weill dyschondrosteosis"
      },
      {
        "code" : "2400",
        "display" : "Peripheral motor neuropathy-dysautonomia syndrome"
      },
      {
        "code" : "240071",
        "display" : "Classic progressive supranuclear palsy syndrome"
      },
      {
        "code" : "240085",
        "display" : "Progressive supranuclear palsy-predominant parkinsonism syndrome"
      },
      {
        "code" : "240094",
        "display" : "Progressive supranuclear palsy-pure akinesia with gait freezing syndrome"
      },
      {
        "code" : "240103",
        "display" : "Progressive supranuclear palsy-corticobasal syndrome"
      },
      {
        "code" : "240112",
        "display" : "Progressive supranuclear palsy-progressive non-fluent aphasia syndrome"
      },
      {
        "code" : "2404",
        "display" : "Loiasis"
      },
      {
        "code" : "2405",
        "display" : "Thickened earlobes-conductive deafness syndrome"
      },
      {
        "code" : "2406",
        "display" : "Locked-in syndrome"
      },
      {
        "code" : "2407",
        "display" : "Laryngo-onycho-cutaneous syndrome"
      },
      {
        "code" : "240760",
        "display" : "Nijmegen breakage syndrome-like disorder"
      },
      {
        "code" : "2408",
        "display" : "Lowe-Kohn-Cohen syndrome"
      },
      {
        "code" : "2409",
        "display" : "Lowry-MacLean syndrome"
      },
      {
        "code" : "241",
        "display" : "Dyschromatosis universalis hereditaria"
      },
      {
        "code" : "2410",
        "display" : "Hypergonadotropic hypogonadism-cataract syndrome"
      },
      {
        "code" : "2412",
        "display" : "Dislocation of the hip-dysmorphism syndrome"
      },
      {
        "code" : "2414",
        "display" : "Congenital pulmonary lymphangiectasia"
      },
      {
        "code" : "242",
        "display" : "46,XY complete gonadal dysgenesis"
      },
      {
        "code" : "2420",
        "display" : "Primary pulmonary lymphoma"
      },
      {
        "code" : "2427",
        "display" : "Macrocephaly-short stature-paraplegia syndrome"
      },
      {
        "code" : "2429",
        "display" : "Macrocephaly-spastic paraplegia-dysmorphism syndrome"
      },
      {
        "code" : "243",
        "display" : "46,XX gonadal dysgenesis"
      },
      {
        "code" : "2430",
        "display" : "Congenital macroglossia"
      },
      {
        "code" : "2432",
        "display" : "Macrosomia-microphthalmia-cleft palate syndrome"
      },
      {
        "code" : "243343",
        "display" : "Dimethylglycine dehydrogenase deficiency"
      },
      {
        "code" : "243367",
        "display" : "Acute fatty liver of pregnancy"
      },
      {
        "code" : "2435",
        "display" : "Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome"
      },
      {
        "code" : "2437",
        "display" : "Czeizel-Losonci syndrome"
      },
      {
        "code" : "2438",
        "display" : "Hand-foot-genital syndrome"
      },
      {
        "code" : "2439",
        "display" : "Patterson-Stevenson-Fontaine syndrome"
      },
      {
        "code" : "244",
        "display" : "Primary ciliary dyskinesia"
      },
      {
        "code" : "2440",
        "display" : "Isolated split hand-split foot malformation"
      },
      {
        "code" : "244242",
        "display" : "HELLP syndrome"
      },
      {
        "code" : "244275",
        "display" : "De novo thrombotic microangiopathy after kidney transplantation"
      },
      {
        "code" : "244283",
        "display" : "Biliary atresia with splenic malformation syndrome"
      },
      {
        "code" : "244305",
        "display" : "Dominant hypophosphatemia with nephrolithiasis or osteoporosis"
      },
      {
        "code" : "244310",
        "display" : "RFT1-CDG"
      },
      {
        "code" : "2444",
        "display" : "Congenital pulmonary airway malformation"
      },
      {
        "code" : "245",
        "display" : "Nager syndrome"
      },
      {
        "code" : "2451",
        "display" : "Mucocutaneous venous malformations"
      },
      {
        "code" : "2456",
        "display" : "Familial supernumerary nipples"
      },
      {
        "code" : "2457",
        "display" : "Mandibuloacral dysplasia"
      },
      {
        "code" : "2459",
        "display" : "Mansonelliasis"
      },
      {
        "code" : "246",
        "display" : "Postaxial acrofacial dysostosis"
      },
      {
        "code" : "2460",
        "display" : "Van den Ende-Gupta syndrome"
      },
      {
        "code" : "2461",
        "display" : "Marden-Walker syndrome"
      },
      {
        "code" : "2462",
        "display" : "Shprintzen-Goldberg syndrome"
      },
      {
        "code" : "2463",
        "display" : "Marfanoid habitus-autosomal recessive intellectual disability syndrome"
      },
      {
        "code" : "2464",
        "display" : "Marfanoid syndrome, De Silva type"
      },
      {
        "code" : "2466",
        "display" : "MASA syndrome"
      },
      {
        "code" : "2470",
        "display" : "Matthew-Wood syndrome"
      },
      {
        "code" : "2471",
        "display" : "McDonough syndrome"
      },
      {
        "code" : "247165",
        "display" : "Infantile mercury poisoning"
      },
      {
        "code" : "247198",
        "display" : "Progressive cerebello-cerebral atrophy"
      },
      {
        "code" : "247203",
        "display" : "Collecting duct carcinoma"
      },
      {
        "code" : "247234",
        "display" : "Sporadic adult-onset ataxia of unknown etiology"
      },
      {
        "code" : "247245",
        "display" : "Superficial siderosis"
      },
      {
        "code" : "247257",
        "display" : "Inhalational anthrax"
      },
      {
        "code" : "247262",
        "display" : "Hyperphosphatasia-intellectual disability syndrome"
      },
      {
        "code" : "2473",
        "display" : "McKusick-Kaufman syndrome"
      },
      {
        "code" : "247353",
        "display" : "Generalized pustular psoriasis"
      },
      {
        "code" : "247378",
        "display" : "Autosomal recessive secondary polycythemia not associated with VHL gene"
      },
      {
        "code" : "2475",
        "display" : "White forelock with malformations"
      },
      {
        "code" : "247511",
        "display" : "Autosomal dominant secondary polycythemia"
      },
      {
        "code" : "247522",
        "display" : "Primary ciliary dyskinesia-retinitis pigmentosa syndrome"
      },
      {
        "code" : "247525",
        "display" : "Citrullinemia type I"
      },
      {
        "code" : "247546",
        "display" : "Acute neonatal citrullinemia type I"
      },
      {
        "code" : "247573",
        "display" : "Late-onset citrullinemia type I"
      },
      {
        "code" : "247585",
        "display" : "Citrullinemia type II"
      },
      {
        "code" : "247598",
        "display" : "Neonatal intrahepatic cholestasis due to citrin deficiency"
      },
      {
        "code" : "2476",
        "display" : "Dysraphism-cleft lip/palate-limb reduction defects syndrome"
      },
      {
        "code" : "247604",
        "display" : "Juvenile primary lateral sclerosis"
      },
      {
        "code" : "247623",
        "display" : "Perinatal lethal hypophosphatasia"
      },
      {
        "code" : "247638",
        "display" : "Prenatal benign hypophosphatasia"
      },
      {
        "code" : "247651",
        "display" : "Infantile hypophosphatasia"
      },
      {
        "code" : "247667",
        "display" : "Childhood-onset hypophosphatasia"
      },
      {
        "code" : "247676",
        "display" : "Adult hypophosphatasia"
      },
      {
        "code" : "247685",
        "display" : "Odontohypophosphatasia"
      },
      {
        "code" : "247691",
        "display" : "Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations"
      },
      {
        "code" : "247698",
        "display" : "Multiple endocrine neoplasia type 2A"
      },
      {
        "code" : "2477",
        "display" : "Isolated megalencephaly"
      },
      {
        "code" : "247709",
        "display" : "Multiple endocrine neoplasia type 2B"
      },
      {
        "code" : "247718",
        "display" : "Inflammatory myopathy with abundant macrophages"
      },
      {
        "code" : "247724",
        "display" : "Idiopathic eosinophilic myositis"
      },
      {
        "code" : "247762",
        "display" : "Lipoblastoma"
      },
      {
        "code" : "247768",
        "display" : "Müllerian aplasia and hyperandrogenism"
      },
      {
        "code" : "247775",
        "display" : "Mayer-Rokitansky-Küster-Hauser syndrome type 1"
      },
      {
        "code" : "247790",
        "display" : "FTH1-related iron overload"
      },
      {
        "code" : "247794",
        "display" : "Juvenile cataract-microcornea-renal glucosuria syndrome"
      },
      {
        "code" : "247798",
        "display" : "MUTYH-related polyposis"
      },
      {
        "code" : "2478",
        "display" : "Megalencephalic leukoencephalopathy with subcortical cysts"
      },
      {
        "code" : "247815",
        "display" : "Autosomal recessive ataxia due to PEX10 deficiency"
      },
      {
        "code" : "247820",
        "display" : "Ectodermal dysplasia-pili torti-cutaneous syndactyly syndrome"
      },
      {
        "code" : "247827",
        "display" : "Ectodermal dysplasia-hyperhidrosis-cutaneous syndactyly syndrome"
      },
      {
        "code" : "247834",
        "display" : "Occult macular dystrophy"
      },
      {
        "code" : "247868",
        "display" : "NLRP12-associated hereditary periodic fever syndrome"
      },
      {
        "code" : "2479",
        "display" : "Megalocornea-intellectual disability syndrome"
      },
      {
        "code" : "248",
        "display" : "Autosomal recessive hypohidrotic ectodermal dysplasia"
      },
      {
        "code" : "2481",
        "display" : "Neurocutaneous melanocytosis"
      },
      {
        "code" : "248111",
        "display" : "Juvenile Huntington disease"
      },
      {
        "code" : "2482",
        "display" : "Melhem-Fahl syndrome"
      },
      {
        "code" : "2483",
        "display" : "Melkersson-Rosenthal syndrome"
      },
      {
        "code" : "248340",
        "display" : "Isolated delta-storage pool disease"
      },
      {
        "code" : "2484",
        "display" : "Melnick-Needles syndrome"
      },
      {
        "code" : "248408",
        "display" : "Familial hypodysfibrinogenemia"
      },
      {
        "code" : "2485",
        "display" : "Melorheostosis"
      },
      {
        "code" : "2487",
        "display" : "Lower limb malformation-hypospadias syndrome"
      },
      {
        "code" : "2489",
        "display" : "Upper limb defect-eye and ear abnormalities syndrome"
      },
      {
        "code" : "249",
        "display" : "Fibrous dysplasia of bone"
      },
      {
        "code" : "2491",
        "display" : "Müllerian duct anomalies-limb anomalies syndrome"
      },
      {
        "code" : "2492",
        "display" : "FATCO syndrome"
      },
      {
        "code" : "2494",
        "display" : "Ménétrier disease"
      },
      {
        "code" : "2495",
        "display" : "Meningioma"
      },
      {
        "code" : "2496",
        "display" : "Mesomelia-synostoses syndrome"
      },
      {
        "code" : "2497",
        "display" : "Upper limb mesomelic dysplasia, type Fryns"
      },
      {
        "code" : "2498",
        "display" : "Syndactyly type 8"
      },
      {
        "code" : "2499",
        "display" : "Metachondromatosis"
      },
      {
        "code" : "25",
        "display" : "Glutaryl-CoA dehydrogenase deficiency"
      },
      {
        "code" : "2500",
        "display" : "Acrogeria"
      },
      {
        "code" : "2501",
        "display" : "Metaphyseal chondrodysplasia, Spahr type"
      },
      {
        "code" : "2502",
        "display" : "Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome"
      },
      {
        "code" : "2504",
        "display" : "Metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome"
      },
      {
        "code" : "2505",
        "display" : "Multiple benign circumferential skin creases on limbs"
      },
      {
        "code" : "2508",
        "display" : "Corpus callosum agenesis-abnormal genitalia syndrome"
      },
      {
        "code" : "250831",
        "display" : "Logopenic progressive aphasia"
      },
      {
        "code" : "250923",
        "display" : "Isolated aniridia"
      },
      {
        "code" : "250932",
        "display" : "Autosomal dominant optic atrophy and peripheral neuropathy"
      },
      {
        "code" : "250972",
        "display" : "Polymicrogyria with optic nerve hypoplasia"
      },
      {
        "code" : "250977",
        "display" : "AICA-ribosiduria"
      },
      {
        "code" : "250984",
        "display" : "Autosomal recessive Stickler syndrome"
      },
      {
        "code" : "250989",
        "display" : "1q21.1 microdeletion syndrome"
      },
      {
        "code" : "250994",
        "display" : "1q21.1 microduplication syndrome"
      },
      {
        "code" : "250999",
        "display" : "1q41q42 microdeletion syndrome"
      },
      {
        "code" : "2510",
        "display" : "Micro syndrome"
      },
      {
        "code" : "251004",
        "display" : "Paternal uniparental disomy of chromosome 1 syndrome"
      },
      {
        "code" : "251009",
        "display" : "Maternal uniparental disomy of chromosome 1 syndrome"
      },
      {
        "code" : "251014",
        "display" : "2q31.1 microdeletion syndrome"
      },
      {
        "code" : "251019",
        "display" : "2q32q33 deletion syndrome"
      },
      {
        "code" : "251028",
        "display" : "SATB2-associated syndrome due to a chromosomal rearrangement"
      },
      {
        "code" : "251038",
        "display" : "3q29 microduplication syndrome"
      },
      {
        "code" : "251043",
        "display" : "Ring chromosome 5 syndrome"
      },
      {
        "code" : "251046",
        "display" : "6p22 microdeletion syndrome"
      },
      {
        "code" : "251056",
        "display" : "6q25.2q25.3 microdeletion syndrome"
      },
      {
        "code" : "251061",
        "display" : "7q31 microdeletion syndrome"
      },
      {
        "code" : "251066",
        "display" : "8p11.2 deletion syndrome"
      },
      {
        "code" : "251071",
        "display" : "8p23.1 microdeletion syndrome"
      },
      {
        "code" : "251076",
        "display" : "8p23.1 duplication syndrome"
      },
      {
        "code" : "2511",
        "display" : "Microbrachycephaly-ptosis-cleft lip syndrome"
      },
      {
        "code" : "2512",
        "display" : "Autosomal recessive primary microcephaly"
      },
      {
        "code" : "251262",
        "display" : "Familial osteochondritis dissecans"
      },
      {
        "code" : "251274",
        "display" : "Familial hyperaldosteronism type III"
      },
      {
        "code" : "251279",
        "display" : "Microphthalmia-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome"
      },
      {
        "code" : "251282",
        "display" : "Autosomal dominant spastic ataxia type 1"
      },
      {
        "code" : "251287",
        "display" : "Benign concentric annular macular dystrophy"
      },
      {
        "code" : "251290",
        "display" : "Parietal foramina with clavicular hypoplasia"
      },
      {
        "code" : "251295",
        "display" : "Pigmented paravenous retinochoroidal atrophy"
      },
      {
        "code" : "2513",
        "display" : "Microcephaly-albinism-digital anomalies syndrome"
      },
      {
        "code" : "251304",
        "display" : "Infantile onset panniculitis with uveitis and systemic granulomatosis"
      },
      {
        "code" : "251307",
        "display" : "Idiopathic recurrent pericarditis"
      },
      {
        "code" : "251325",
        "display" : "Drug-induced vasculitis"
      },
      {
        "code" : "251328",
        "display" : "Unclassified vasculitis"
      },
      {
        "code" : "251332",
        "display" : "Unexplained long-lasting fever/inflammatory syndrome"
      },
      {
        "code" : "251347",
        "display" : "Ataxia-telangiectasia-like disorder"
      },
      {
        "code" : "251359",
        "display" : "Sickle cell-beta-thalassemia disease syndrome"
      },
      {
        "code" : "251365",
        "display" : "Sickle cell S-C disease"
      },
      {
        "code" : "251370",
        "display" : "Sickle cell S-D Punjab disease"
      },
      {
        "code" : "251375",
        "display" : "Sickle cell S-E disease"
      },
      {
        "code" : "251380",
        "display" : "Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome"
      },
      {
        "code" : "251383",
        "display" : "CK syndrome"
      },
      {
        "code" : "251393",
        "display" : "Localized junctional epidermolysis bullosa"
      },
      {
        "code" : "2514",
        "display" : "Autosomal dominant primary microcephaly"
      },
      {
        "code" : "2515",
        "display" : "Microcephaly-cardiomyopathy syndrome"
      },
      {
        "code" : "251510",
        "display" : "46,XY partial gonadal dysgenesis"
      },
      {
        "code" : "251515",
        "display" : "Distal arthrogryposis type 10"
      },
      {
        "code" : "251523",
        "display" : "Hyperzincemia and hypercalprotectinemia"
      },
      {
        "code" : "251576",
        "display" : "Gliosarcoma"
      },
      {
        "code" : "251579",
        "display" : "Giant cell glioblastoma"
      },
      {
        "code" : "251582",
        "display" : "Gliomatosis cerebri"
      },
      {
        "code" : "251589",
        "display" : "Anaplastic astrocytoma"
      },
      {
        "code" : "251595",
        "display" : "Diffuse astrocytoma"
      },
      {
        "code" : "251598",
        "display" : "Protoplasmic astrocytoma"
      },
      {
        "code" : "2516",
        "display" : "Microcephaly-cardiac defect-lung malsegmentation syndrome"
      },
      {
        "code" : "251601",
        "display" : "Fibrillary astrocytoma"
      },
      {
        "code" : "251604",
        "display" : "Gemistocytic astrocytoma"
      },
      {
        "code" : "251607",
        "display" : "Pleomorphic xanthoastrocytoma"
      },
      {
        "code" : "251612",
        "display" : "Pilocytic astrocytoma"
      },
      {
        "code" : "251615",
        "display" : "Pilomyxoid astrocytoma"
      },
      {
        "code" : "251618",
        "display" : "Subependymal giant cell astrocytoma"
      },
      {
        "code" : "251623",
        "display" : "Pituicytoma"
      },
      {
        "code" : "251627",
        "display" : "Oligodendroglioma"
      },
      {
        "code" : "251630",
        "display" : "Anaplastic oligodendroglioma"
      },
      {
        "code" : "251636",
        "display" : "Ependymoma"
      },
      {
        "code" : "251639",
        "display" : "Subependymoma"
      },
      {
        "code" : "251643",
        "display" : "Myxopapillary ependymoma"
      },
      {
        "code" : "251646",
        "display" : "Anaplastic ependymoma"
      },
      {
        "code" : "251656",
        "display" : "Oligoastrocytoma"
      },
      {
        "code" : "251663",
        "display" : "Anaplastic oligoastrocytoma"
      },
      {
        "code" : "251671",
        "display" : "Angiocentric glioma"
      },
      {
        "code" : "251674",
        "display" : "Chordoid glioma"
      },
      {
        "code" : "251679",
        "display" : "Astroblastoma"
      },
      {
        "code" : "2518",
        "display" : "Autosomal recessive chorioretinopathy-microcephaly syndrome"
      },
      {
        "code" : "251855",
        "display" : "Anaplastic/large cell medulloblastoma"
      },
      {
        "code" : "251858",
        "display" : "Medulloblastoma with extensive nodularity"
      },
      {
        "code" : "251863",
        "display" : "Desmoplastic/nodular medulloblastoma"
      },
      {
        "code" : "251867",
        "display" : "Classic medulloblastoma"
      },
      {
        "code" : "251877",
        "display" : "Ganglioneuroblastoma"
      },
      {
        "code" : "251899",
        "display" : "Choroid plexus carcinoma"
      },
      {
        "code" : "2519",
        "display" : "Microcephaly-seizures-intellectual disability-heart disease syndrome"
      },
      {
        "code" : "251902",
        "display" : "Atypical papilloma of choroid plexus"
      },
      {
        "code" : "251909",
        "display" : "Pineoblastoma"
      },
      {
        "code" : "251912",
        "display" : "Pineocytoma"
      },
      {
        "code" : "251915",
        "display" : "Papillary tumor of the pineal region"
      },
      {
        "code" : "251919",
        "display" : "Pineal parenchymal tumor of intermediate differentiation"
      },
      {
        "code" : "251927",
        "display" : "Extraventricular neurocytoma"
      },
      {
        "code" : "251931",
        "display" : "Cerebellar liponeurocytoma"
      },
      {
        "code" : "251937",
        "display" : "Gangliocytoma"
      },
      {
        "code" : "251940",
        "display" : "Desmoplastic infantile astrocytoma/ganglioglioma"
      },
      {
        "code" : "251946",
        "display" : "Dysembryoplastic neuroepithelial tumor"
      },
      {
        "code" : "251949",
        "display" : "Ganglioglioma"
      },
      {
        "code" : "251957",
        "display" : "Anaplastic ganglioglioma"
      },
      {
        "code" : "251962",
        "display" : "Papillary glioneuronal tumor"
      },
      {
        "code" : "251975",
        "display" : "Rosette-forming glioneuronal tumor"
      },
      {
        "code" : "251992",
        "display" : "Ganglioneuroma"
      },
      {
        "code" : "252006",
        "display" : "Yolk sac tumor of central nervous system"
      },
      {
        "code" : "252015",
        "display" : "Choriocarcinoma of the central nervous system"
      },
      {
        "code" : "252018",
        "display" : "Teratoma of the central nervous system"
      },
      {
        "code" : "252021",
        "display" : "Mixed germ cell tumor of central nervous system"
      },
      {
        "code" : "252031",
        "display" : "Diffuse leptomeningeal melanocytosis"
      },
      {
        "code" : "252046",
        "display" : "Meningeal melanocytoma"
      },
      {
        "code" : "252050",
        "display" : "Primary melanoma of the central nervous system"
      },
      {
        "code" : "252054",
        "display" : "Hemangioblastoma"
      },
      {
        "code" : "2521",
        "display" : "Microcephaly-cleft palate-abnormal retinal pigmentation syndrome"
      },
      {
        "code" : "252128",
        "display" : "Malignant peripheral nerve sheath tumor with perineurial differentiation"
      },
      {
        "code" : "252164",
        "display" : "Benign schwannoma"
      },
      {
        "code" : "252175",
        "display" : "Vestibular schwannoma"
      },
      {
        "code" : "252183",
        "display" : "Neurofibroma"
      },
      {
        "code" : "2522",
        "display" : "Microcephaly-cervical spine fusion anomalies syndrome"
      },
      {
        "code" : "252202",
        "display" : "Constitutional mismatch repair deficiency syndrome"
      },
      {
        "code" : "252206",
        "display" : "Melanoma and neural system tumor syndrome"
      },
      {
        "code" : "252212",
        "display" : "Malignant triton tumor"
      },
      {
        "code" : "2523",
        "display" : "Microcephaly-brain defect-spasticity-hypernatremia syndrome"
      },
      {
        "code" : "2524",
        "display" : "Pontocerebellar hypoplasia type 2"
      },
      {
        "code" : "2526",
        "display" : "Microcephaly-lymphedema-chorioretinopathy syndrome"
      },
      {
        "code" : "2528",
        "display" : "Microcephaly-microcornea syndrome, Seemanova type"
      },
      {
        "code" : "2533",
        "display" : "Microcephaly-deafness-intellectual disability syndrome"
      },
      {
        "code" : "2536",
        "display" : "Microcornea-glaucoma-absent frontal sinuses syndrome"
      },
      {
        "code" : "2538",
        "display" : "Microgastria-limb reduction defect syndrome"
      },
      {
        "code" : "254334",
        "display" : "Autosomal recessive intermediate Charcot-Marie-Tooth disease type B"
      },
      {
        "code" : "254343",
        "display" : "Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome"
      },
      {
        "code" : "254346",
        "display" : "19p13.12 microdeletion syndrome"
      },
      {
        "code" : "254351",
        "display" : "Distal 7q11.23 microdeletion syndrome"
      },
      {
        "code" : "254361",
        "display" : "Plectin-related limb-girdle muscular dystrophy R17"
      },
      {
        "code" : "254379",
        "display" : "Linear lichen planus"
      },
      {
        "code" : "254395",
        "display" : "Actinic lichen planus"
      },
      {
        "code" : "254411",
        "display" : "Annular atrophic lichen planus"
      },
      {
        "code" : "254424",
        "display" : "Annular lichen planus"
      },
      {
        "code" : "254449",
        "display" : "Atrophic lichen planus"
      },
      {
        "code" : "254463",
        "display" : "Lichen planus pigmentosus"
      },
      {
        "code" : "254478",
        "display" : "Lichen planus pemphigoides"
      },
      {
        "code" : "254492",
        "display" : "Frontal fibrosing alopecia"
      },
      {
        "code" : "254504",
        "display" : "Inhalational botulism"
      },
      {
        "code" : "254509",
        "display" : "Iatrogenic botulism"
      },
      {
        "code" : "254516",
        "display" : "Temple syndrome"
      },
      {
        "code" : "254519",
        "display" : "Kagami-Ogata syndrome"
      },
      {
        "code" : "254525",
        "display" : "Temple syndrome due to paternal 14q32.2 microdeletion"
      },
      {
        "code" : "254528",
        "display" : "Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion"
      },
      {
        "code" : "254531",
        "display" : "Temple syndrome due to paternal 14q32.2 hypomethylation"
      },
      {
        "code" : "254534",
        "display" : "Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation"
      },
      {
        "code" : "254688",
        "display" : "Complete hydatidiform mole"
      },
      {
        "code" : "254693",
        "display" : "Partial hydatidiform mole"
      },
      {
        "code" : "254698",
        "display" : "Epithelioid trophoblastic tumor"
      },
      {
        "code" : "2547",
        "display" : "Microphthalmia-microtia-fetal akinesia syndrome"
      },
      {
        "code" : "254704",
        "display" : "Genetic hyperferritinemia without iron overload"
      },
      {
        "code" : "254851",
        "display" : "Mitochondrial DNA-related dystonia"
      },
      {
        "code" : "254854",
        "display" : "Pure mitochondrial myopathy"
      },
      {
        "code" : "254857",
        "display" : "Lethal infantile mitochondrial myopathy"
      },
      {
        "code" : "254864",
        "display" : "Mitochondrial myopathy with reversible cytochrome C oxidase deficiency"
      },
      {
        "code" : "254875",
        "display" : "Mitochondrial DNA depletion syndrome, myopathic form"
      },
      {
        "code" : "254881",
        "display" : "Spinocerebellar ataxia with epilepsy"
      },
      {
        "code" : "254886",
        "display" : "Autosomal recessive progressive external ophthalmoplegia"
      },
      {
        "code" : "254892",
        "display" : "Autosomal dominant progressive external ophthalmoplegia"
      },
      {
        "code" : "254898",
        "display" : "Deafness-encephaloneuropathy-obesity-valvulopathy syndrome"
      },
      {
        "code" : "2549",
        "display" : "Oculoauriculovertebral spectrum with radial defects"
      },
      {
        "code" : "254902",
        "display" : "Renal tubulopathy-encephalopathy-liver failure syndrome"
      },
      {
        "code" : "254905",
        "display" : "Isolated cytochrome C oxidase deficiency"
      },
      {
        "code" : "254913",
        "display" : "Isolated ATP synthase deficiency"
      },
      {
        "code" : "254920",
        "display" : "Combined oxidative phosphorylation defect type 2"
      },
      {
        "code" : "254925",
        "display" : "Combined oxidative phosphorylation defect type 4"
      },
      {
        "code" : "254930",
        "display" : "Combined oxidative phosphorylation defect type 7"
      },
      {
        "code" : "2551",
        "display" : "Microspherophakia-metaphyseal dysplasia syndrome"
      },
      {
        "code" : "255132",
        "display" : "Adult-onset autosomal recessive sideroblastic anemia"
      },
      {
        "code" : "255138",
        "display" : "Pyruvate dehydrogenase E1-beta deficiency"
      },
      {
        "code" : "255182",
        "display" : "Pyruvate dehydrogenase E3-binding protein deficiency"
      },
      {
        "code" : "2552",
        "display" : "Microsporidiosis"
      },
      {
        "code" : "255210",
        "display" : "Mitochondrial DNA-associated Leigh syndrome"
      },
      {
        "code" : "255229",
        "display" : "Navajo neurohepatopathy"
      },
      {
        "code" : "255235",
        "display" : "Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy"
      },
      {
        "code" : "2554",
        "display" : "Ear-patella-short stature syndrome"
      },
      {
        "code" : "2556",
        "display" : "Microphthalmia with linear skin defects syndrome"
      },
      {
        "code" : "2557",
        "display" : "Mietens syndrome"
      },
      {
        "code" : "2558",
        "display" : "Mikati-Najjar-Sahli syndrome"
      },
      {
        "code" : "256",
        "display" : "Early-onset generalized limb-onset dystonia"
      },
      {
        "code" : "2560",
        "display" : "Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome"
      },
      {
        "code" : "2561",
        "display" : "Pyramidal molars-abnormal upper lip syndrome"
      },
      {
        "code" : "2563",
        "display" : "MOMO syndrome"
      },
      {
        "code" : "2564",
        "display" : "Tetramelic monodactyly"
      },
      {
        "code" : "2565",
        "display" : "Mononen-Karnes-Senac syndrome"
      },
      {
        "code" : "2566",
        "display" : "Chronic Epstein-Barr virus infection syndrome"
      },
      {
        "code" : "257",
        "display" : "Epidermolysis bullosa simplex with muscular dystrophy"
      },
      {
        "code" : "2570",
        "display" : "Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome"
      },
      {
        "code" : "2571",
        "display" : "X-linked immunoneurologic disorder"
      },
      {
        "code" : "2572",
        "display" : "Spastic ataxia-corneal dystrophy syndrome"
      },
      {
        "code" : "2573",
        "display" : "Moyamoya disease"
      },
      {
        "code" : "2574",
        "display" : "Moynahan syndrome"
      },
      {
        "code" : "2575",
        "display" : "Cystic fibrosis-gastritis-megaloblastic anemia syndrome"
      },
      {
        "code" : "2576",
        "display" : "Mulibrey nanism"
      },
      {
        "code" : "2578",
        "display" : "Mayer-Rokitansky-Küster-Hauser syndrome type 2"
      },
      {
        "code" : "2579",
        "display" : "Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome"
      },
      {
        "code" : "258",
        "display" : "Laminin subunit alpha 2-related congenital muscular dystrophy"
      },
      {
        "code" : "2582",
        "display" : "Myalgia-eosinophilia syndrome associated with tryptophan"
      },
      {
        "code" : "2583",
        "display" : "Mycetoma"
      },
      {
        "code" : "2584",
        "display" : "Classic mycosis fungoides"
      },
      {
        "code" : "2585",
        "display" : "Ataxia-pancytopenia syndrome"
      },
      {
        "code" : "2587",
        "display" : "Myeloperoxidase deficiency"
      },
      {
        "code" : "2588",
        "display" : "Myhre syndrome"
      },
      {
        "code" : "2589",
        "display" : "Myoclonus-cerebellar ataxia-deafness syndrome"
      },
      {
        "code" : "2590",
        "display" : "Spinal muscular atrophy-progressive myoclonic epilepsy syndrome"
      },
      {
        "code" : "2591",
        "display" : "Infantile myofibromatosis"
      },
      {
        "code" : "2593",
        "display" : "Tubular aggregate myopathy"
      },
      {
        "code" : "2596",
        "display" : "Myopathy and diabetes mellitus"
      },
      {
        "code" : "25968",
        "display" : "Self-limited childhood occipital epilepsy"
      },
      {
        "code" : "2597",
        "display" : "Mitochondrial myopathy-lactic acidosis-deafness syndrome"
      },
      {
        "code" : "2598",
        "display" : "Mitochondrial myopathy and sideroblastic anemia"
      },
      {
        "code" : "25980",
        "display" : "X-linked myopathy with excessive autophagy"
      },
      {
        "code" : "26",
        "display" : "Methylmalonic acidemia with homocystinuria"
      },
      {
        "code" : "260305",
        "display" : "Autosomal recessive sideroblastic anemia"
      },
      {
        "code" : "2604",
        "display" : "Familial visceral myopathy"
      },
      {
        "code" : "2608",
        "display" : "N syndrome"
      },
      {
        "code" : "2609",
        "display" : "Isolated complex I deficiency"
      },
      {
        "code" : "261",
        "display" : "Emery-Dreifuss muscular dystrophy"
      },
      {
        "code" : "26106",
        "display" : "Hereditary diffuse gastric cancer"
      },
      {
        "code" : "2611",
        "display" : "Linear verrucous nevus syndrome"
      },
      {
        "code" : "261102",
        "display" : "Distal 7q11.23 microduplication syndrome"
      },
      {
        "code" : "261112",
        "display" : "Monosomy 9p syndrome"
      },
      {
        "code" : "261120",
        "display" : "14q11.2 microdeletion syndrome"
      },
      {
        "code" : "261144",
        "display" : "FOXG1 syndrome due to 14q12 microdeletion"
      },
      {
        "code" : "261183",
        "display" : "15q11.2 microdeletion syndrome"
      },
      {
        "code" : "261190",
        "display" : "Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion"
      },
      {
        "code" : "261197",
        "display" : "Proximal 16p11.2 microdeletion syndrome"
      },
      {
        "code" : "2612",
        "display" : "Linear nevus sebaceus syndrome"
      },
      {
        "code" : "261204",
        "display" : "16p11.2p12.2 microduplication syndrome"
      },
      {
        "code" : "261211",
        "display" : "16p11.2p12.2 microdeletion syndrome"
      },
      {
        "code" : "261222",
        "display" : "Distal 16p11.2 microdeletion syndrome"
      },
      {
        "code" : "261229",
        "display" : "14q11.2 microduplication syndrome"
      },
      {
        "code" : "261236",
        "display" : "16p13.11 microdeletion syndrome"
      },
      {
        "code" : "261243",
        "display" : "16p13.11 microduplication syndrome"
      },
      {
        "code" : "261250",
        "display" : "16q24.3 microdeletion syndrome"
      },
      {
        "code" : "261257",
        "display" : "Distal 17p13.3 microdeletion syndrome"
      },
      {
        "code" : "261265",
        "display" : "17q12 microdeletion syndrome"
      },
      {
        "code" : "261272",
        "display" : "17q12 microduplication syndrome"
      },
      {
        "code" : "261279",
        "display" : "17q23.1q23.2 microdeletion syndrome"
      },
      {
        "code" : "261290",
        "display" : "Trisomy 17p syndrome"
      },
      {
        "code" : "261295",
        "display" : "20p12.3 microdeletion syndrome"
      },
      {
        "code" : "2613",
        "display" : "Nail-patella-like renal disease"
      },
      {
        "code" : "261304",
        "display" : "Paternal 20q13.2q13.3 microdeletion syndrome"
      },
      {
        "code" : "261311",
        "display" : "20q13.33 microdeletion syndrome"
      },
      {
        "code" : "261318",
        "display" : "Trisomy 20p syndrome"
      },
      {
        "code" : "261323",
        "display" : "21q22.11q22.12 microdeletion syndrome"
      },
      {
        "code" : "261330",
        "display" : "Distal 22q11.2 microdeletion syndrome"
      },
      {
        "code" : "261337",
        "display" : "Distal 22q11.2 microduplication syndrome"
      },
      {
        "code" : "261344",
        "display" : "Trisomy 1q syndrome"
      },
      {
        "code" : "261349",
        "display" : "2p15p16.1 microdeletion syndrome"
      },
      {
        "code" : "26137",
        "display" : "Juvenile temporal arteritis"
      },
      {
        "code" : "2614",
        "display" : "Nail-patella syndrome"
      },
      {
        "code" : "261476",
        "display" : "Xp21 deletion syndrome"
      },
      {
        "code" : "261483",
        "display" : "Xq27.3q28 duplication syndrome"
      },
      {
        "code" : "261494",
        "display" : "Kleefstra syndrome"
      },
      {
        "code" : "261501",
        "display" : "Atypical Norrie disease due to Xp11.3 microdeletion"
      },
      {
        "code" : "261519",
        "display" : "Maternal uniparental disomy of chromosome X syndrome"
      },
      {
        "code" : "261524",
        "display" : "Paternal uniparental disomy of chromosome X syndrome"
      },
      {
        "code" : "261529",
        "display" : "Ring chromosome Y syndrome"
      },
      {
        "code" : "261534",
        "display" : "49,XXXYY syndrome"
      },
      {
        "code" : "261537",
        "display" : "Mowat-Wilson syndrome due to monosomy 2q22"
      },
      {
        "code" : "261552",
        "display" : "Mowat-Wilson syndrome due to a ZEB2 point mutation"
      },
      {
        "code" : "261584",
        "display" : "5q22 microdeletion syndrome"
      },
      {
        "code" : "2616",
        "display" : "3M syndrome"
      },
      {
        "code" : "261600",
        "display" : "Alagille syndrome due to 20p12 microdeletion"
      },
      {
        "code" : "261619",
        "display" : "Alagille syndrome due to a JAG1 point mutation"
      },
      {
        "code" : "261629",
        "display" : "Alagille syndrome due to a NOTCH2 point mutation"
      },
      {
        "code" : "261638",
        "display" : "Okihiro syndrome due to 20q13 microdeletion"
      },
      {
        "code" : "261647",
        "display" : "Okihiro syndrome due to a point mutation"
      },
      {
        "code" : "261652",
        "display" : "Kleefstra syndrome due to a point mutation"
      },
      {
        "code" : "2617",
        "display" : "Microcephalic primordial dwarfism, Montreal type"
      },
      {
        "code" : "2619",
        "display" : "Brachydactylous dwarfism, Mseleni type"
      },
      {
        "code" : "2623",
        "display" : "Geleophysic dysplasia"
      },
      {
        "code" : "2631",
        "display" : "Mesomelic dwarfism-cleft palate-camptodactyly syndrome"
      },
      {
        "code" : "2632",
        "display" : "Langer mesomelic dysplasia"
      },
      {
        "code" : "263297",
        "display" : "Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency"
      },
      {
        "code" : "2633",
        "display" : "Mesomelic dysplasia, Nievergelt type"
      },
      {
        "code" : "263310",
        "display" : "Thymoma type A"
      },
      {
        "code" : "263317",
        "display" : "Thymoma type B"
      },
      {
        "code" : "263324",
        "display" : "Thymoma type AB"
      },
      {
        "code" : "263331",
        "display" : "Well-differentiated thymic neuroendocrine carcinoma"
      },
      {
        "code" : "263335",
        "display" : "Moderately-differentiated thymic neuroendocrine carcinoma"
      },
      {
        "code" : "263339",
        "display" : "Poorly differentiated thymic neuroendocrine carcinoma"
      },
      {
        "code" : "263347",
        "display" : "MRCS syndrome"
      },
      {
        "code" : "263352",
        "display" : "Postcardiotomy right ventricular failure"
      },
      {
        "code" : "2634",
        "display" : "Mesomelic dwarfism, Reinhardt-Pfeiffer type"
      },
      {
        "code" : "263410",
        "display" : "Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome"
      },
      {
        "code" : "263413",
        "display" : "Angiosarcoma"
      },
      {
        "code" : "263425",
        "display" : "Nevus of Ota"
      },
      {
        "code" : "263432",
        "display" : "Nevus of Ito"
      },
      {
        "code" : "263435",
        "display" : "Congenital smooth muscle hamartoma"
      },
      {
        "code" : "263455",
        "display" : "Congenital hyperinsulinism due to HNF4A deficiency"
      },
      {
        "code" : "263458",
        "display" : "Hyperinsulinism due to INSR deficiency"
      },
      {
        "code" : "263463",
        "display" : "CHST3-related skeletal dysplasia"
      },
      {
        "code" : "263479",
        "display" : "Fuchs heterochromic iridocyclitis"
      },
      {
        "code" : "26348",
        "display" : "Acquired prothrombin deficiency"
      },
      {
        "code" : "263482",
        "display" : "Spondyloepimetaphyseal dysplasia, Maroteaux type"
      },
      {
        "code" : "263487",
        "display" : "COG5-CDG"
      },
      {
        "code" : "26349",
        "display" : "Protein S acquired deficiency"
      },
      {
        "code" : "263494",
        "display" : "DPM3-CDG"
      },
      {
        "code" : "2635",
        "display" : "Metatropic dysplasia"
      },
      {
        "code" : "263501",
        "display" : "COG4-CDG"
      },
      {
        "code" : "263508",
        "display" : "COG1-CDG"
      },
      {
        "code" : "263516",
        "display" : "Progressive myoclonic epilepsy type 3"
      },
      {
        "code" : "263524",
        "display" : "Acute necrotizing encephalopathy of childhood"
      },
      {
        "code" : "263534",
        "display" : "Acral peeling skin syndrome"
      },
      {
        "code" : "263543",
        "display" : "Generalized peeling skin syndrome"
      },
      {
        "code" : "263548",
        "display" : "Peeling skin syndrome type A"
      },
      {
        "code" : "263553",
        "display" : "Peeling skin syndrome type B"
      },
      {
        "code" : "2636",
        "display" : "Microcephalic osteodysplastic primordial dwarfism types I and III"
      },
      {
        "code" : "263662",
        "display" : "Familial multiple meningioma"
      },
      {
        "code" : "263665",
        "display" : "NK-cell enteropathy"
      },
      {
        "code" : "2637",
        "display" : "Microcephalic osteodysplastic primordial dwarfism type II"
      },
      {
        "code" : "2639",
        "display" : "Fibular aplasia-complex brachydactyly syndrome"
      },
      {
        "code" : "264200",
        "display" : "14q22q23 microdeletion syndrome"
      },
      {
        "code" : "2643",
        "display" : "Microcephalic primordial dwarfism, Toriello type"
      },
      {
        "code" : "264450",
        "display" : "Trisomy 8p syndrome"
      },
      {
        "code" : "2645",
        "display" : "Osteoglosphonic dysplasia"
      },
      {
        "code" : "264580",
        "display" : "Glycogen storage disease due to liver phosphorylase kinase deficiency"
      },
      {
        "code" : "264675",
        "display" : "Hereditary pulmonary alveolar proteinosis"
      },
      {
        "code" : "264688",
        "display" : "Congenital chylothorax"
      },
      {
        "code" : "264691",
        "display" : "Isolated pulmonary capillaritis"
      },
      {
        "code" : "264978",
        "display" : "Drug or radiation exposure-related interstitial lung disease"
      },
      {
        "code" : "2655",
        "display" : "Thanatophoric dysplasia"
      },
      {
        "code" : "2658",
        "display" : "Lenz-Majewski hyperostotic dwarfism"
      },
      {
        "code" : "2662",
        "display" : "Keipert syndrome"
      },
      {
        "code" : "2663",
        "display" : "Nathalie syndrome"
      },
      {
        "code" : "2665",
        "display" : "Congenital mesoblastic nephroma"
      },
      {
        "code" : "2666",
        "display" : "Adult familial nephronophthisis-spastic quadriparesia syndrome"
      },
      {
        "code" : "2668",
        "display" : "Nephropathy-deafness-hyperparathyroidism syndrome"
      },
      {
        "code" : "2669",
        "display" : "Nephrosis-deafness-urinary tract-digital malformations syndrome"
      },
      {
        "code" : "267",
        "display" : "Calpain-3-related limb-girdle muscular dystrophy R1"
      },
      {
        "code" : "2670",
        "display" : "Pierson syndrome"
      },
      {
        "code" : "2671",
        "display" : "Neu-Laxova syndrome"
      },
      {
        "code" : "2672",
        "display" : "Neuhauser-Eichner-Opitz syndrome"
      },
      {
        "code" : "2673",
        "display" : "Neurofaciodigitorenal syndrome"
      },
      {
        "code" : "2674",
        "display" : "Cyprus facial-neuromusculoskeletal syndrome"
      },
      {
        "code" : "2678",
        "display" : "Familial isolated café-au-lait macules"
      },
      {
        "code" : "26790",
        "display" : "Pseudomyxoma peritonei"
      },
      {
        "code" : "26791",
        "display" : "Multiple acyl-CoA dehydrogenase deficiency"
      },
      {
        "code" : "26792",
        "display" : "Short chain acyl-CoA dehydrogenase deficiency"
      },
      {
        "code" : "26793",
        "display" : "Very long chain acyl-CoA dehydrogenase deficiency"
      },
      {
        "code" : "268",
        "display" : "Dysferlin-related limb-girdle muscular dystrophy R2"
      },
      {
        "code" : "2680",
        "display" : "Hypomyelination neuropathy-arthrogryposis syndrome"
      },
      {
        "code" : "268114",
        "display" : "RAS-associated autoimmune leukoproliferative disease"
      },
      {
        "code" : "268129",
        "display" : "Spheroid body myopathy"
      },
      {
        "code" : "268139",
        "display" : "Intraocular medulloepithelioma"
      },
      {
        "code" : "268145",
        "display" : "Classic maple syrup urine disease"
      },
      {
        "code" : "268162",
        "display" : "Intermediate maple syrup urine disease"
      },
      {
        "code" : "268173",
        "display" : "Intermittent maple syrup urine disease"
      },
      {
        "code" : "268184",
        "display" : "Thiamine-responsive maple syrup urine disease"
      },
      {
        "code" : "268249",
        "display" : "Mycophenolate mofetil embryopathy"
      },
      {
        "code" : "268261",
        "display" : "DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion"
      },
      {
        "code" : "268316",
        "display" : "Complication in hemodialysis"
      },
      {
        "code" : "268322",
        "display" : "Hereditary thrombocytopenia with normal platelets"
      },
      {
        "code" : "268363",
        "display" : "Open iniencephaly"
      },
      {
        "code" : "268366",
        "display" : "Closed iniencephaly"
      },
      {
        "code" : "2686",
        "display" : "Cyclic neutropenia"
      },
      {
        "code" : "2688",
        "display" : "Adult idiopathic neutropenia"
      },
      {
        "code" : "268810",
        "display" : "Isolated posterior meningocele"
      },
      {
        "code" : "268820",
        "display" : "Cranial meningocele"
      },
      {
        "code" : "268823",
        "display" : "Occipital encephalocele"
      },
      {
        "code" : "268826",
        "display" : "Parietal encephalocele"
      },
      {
        "code" : "268829",
        "display" : "Basal encephalocele"
      },
      {
        "code" : "268861",
        "display" : "Primary tethered cord syndrome"
      },
      {
        "code" : "268865",
        "display" : "Neurenteric cyst"
      },
      {
        "code" : "268868",
        "display" : "Isolated amyelia"
      },
      {
        "code" : "268882",
        "display" : "Arnold-Chiari malformation type I"
      },
      {
        "code" : "268936",
        "display" : "Isolated arhinencephaly"
      },
      {
        "code" : "268940",
        "display" : "Bilateral polymicrogyria"
      },
      {
        "code" : "268943",
        "display" : "Unilateral polymicrogyria"
      },
      {
        "code" : "268947",
        "display" : "Unilateral focal polymicrogyria"
      },
      {
        "code" : "268961",
        "display" : "Isolated focal cortical dysplasia type I"
      },
      {
        "code" : "268973",
        "display" : "Isolated focal cortical dysplasia type Ia"
      },
      {
        "code" : "268980",
        "display" : "Isolated focal cortical dysplasia type Ib"
      },
      {
        "code" : "268987",
        "display" : "Isolated focal cortical dysplasia type Ic"
      },
      {
        "code" : "268994",
        "display" : "Isolated focal cortical dysplasia type II"
      },
      {
        "code" : "269",
        "display" : "Facioscapulohumeral dystrophy"
      },
      {
        "code" : "2690",
        "display" : "Neutropenia-monocytopenia-deafness syndrome"
      },
      {
        "code" : "269001",
        "display" : "Isolated focal cortical dysplasia type IIa"
      },
      {
        "code" : "269008",
        "display" : "Isolated focal cortical dysplasia type IIb"
      },
      {
        "code" : "269197",
        "display" : "Glioependymal/ependymal cyst"
      },
      {
        "code" : "269203",
        "display" : "Isolated cerebellar vermis agenesis"
      },
      {
        "code" : "269206",
        "display" : "Isolated total cerebellar vermis agenesis"
      },
      {
        "code" : "269209",
        "display" : "Isolated partial cerebellar vermis agenesis"
      },
      {
        "code" : "269212",
        "display" : "Isolated Dandy-Walker malformation with hydrocephalus"
      },
      {
        "code" : "269215",
        "display" : "Isolated Dandy-Walker malformation without hydrocephalus"
      },
      {
        "code" : "269218",
        "display" : "Isolated unilateral hemispheric cerebellar hypoplasia"
      },
      {
        "code" : "269221",
        "display" : "Isolated bilateral hemispheric cerebellar hypoplasia"
      },
      {
        "code" : "269229",
        "display" : "Pontine tegmental cap dysplasia"
      },
      {
        "code" : "2695",
        "display" : "Bifid nose"
      },
      {
        "code" : "269505",
        "display" : "Congenital communicating hydrocephalus"
      },
      {
        "code" : "269510",
        "display" : "Congenital non-communicating hydrocephalus"
      },
      {
        "code" : "2697",
        "display" : "Arthrogryposis-renal dysfunction-cholestasis syndrome"
      },
      {
        "code" : "2698",
        "display" : "Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome"
      },
      {
        "code" : "2699",
        "display" : "Median nodule of the upper lip"
      },
      {
        "code" : "27",
        "display" : "Vitamin B12-unresponsive methylmalonic acidemia"
      },
      {
        "code" : "270",
        "display" : "Oculopharyngeal muscular dystrophy"
      },
      {
        "code" : "2700",
        "display" : "Noma"
      },
      {
        "code" : "2701",
        "display" : "Noonan syndrome-like disorder with loose anagen hair"
      },
      {
        "code" : "2703",
        "display" : "Port-wine nevi-mega cisterna magna-hydrocephalus syndrome"
      },
      {
        "code" : "2704",
        "display" : "Urofacial syndrome"
      },
      {
        "code" : "2707",
        "display" : "Oculocerebrofacial syndrome, Kaufman type"
      },
      {
        "code" : "2709",
        "display" : "Oculodental syndrome, Rutherfurd type"
      },
      {
        "code" : "2710",
        "display" : "Oculodentodigital dysplasia"
      },
      {
        "code" : "2712",
        "display" : "Oculofaciocardiodental syndrome"
      },
      {
        "code" : "2713",
        "display" : "Oculoosteocutaneous syndrome"
      },
      {
        "code" : "2714",
        "display" : "Oculo-palato-cerebral syndrome"
      },
      {
        "code" : "2715",
        "display" : "Severe oculo-renal-cerebellar syndrome"
      },
      {
        "code" : "2717",
        "display" : "Oculotrichoanal syndrome"
      },
      {
        "code" : "2718",
        "display" : "Oculotrichodysplasia"
      },
      {
        "code" : "271861",
        "display" : "Hereditary ATTR amyloidosis"
      },
      {
        "code" : "2719",
        "display" : "Oculocerebral hypopigmentation syndrome, Cross type"
      },
      {
        "code" : "272",
        "display" : "Congenital muscular dystrophy, Fukuyama type"
      },
      {
        "code" : "2720",
        "display" : "Oculocerebral hypopigmentation syndrome, Preus type"
      },
      {
        "code" : "2721",
        "display" : "Odonto-onycho-dermal dysplasia"
      },
      {
        "code" : "2722",
        "display" : "Odonto-onycho dysplasia-alopecia syndrome"
      },
      {
        "code" : "2723",
        "display" : "Odontotrichomelic syndrome"
      },
      {
        "code" : "2724",
        "display" : "Odontomatosis-aortae esophagus stenosis syndrome"
      },
      {
        "code" : "2728",
        "display" : "Blepharophimosis-intellectual disability syndrome, Ohdo type"
      },
      {
        "code" : "273",
        "display" : "Steinert myotonic dystrophy"
      },
      {
        "code" : "2730",
        "display" : "Postaxial tetramelic oligodactyly"
      },
      {
        "code" : "2732",
        "display" : "Olivopontocerebellar atrophy-deafness syndrome"
      },
      {
        "code" : "2733",
        "display" : "Omodysplasia"
      },
      {
        "code" : "2736",
        "display" : "Lethal omphalocele-cleft palate syndrome"
      },
      {
        "code" : "2737",
        "display" : "Onchocerciasis"
      },
      {
        "code" : "274",
        "display" : "Bernard-Soulier syndrome"
      },
      {
        "code" : "2741",
        "display" : "Ophthalmomandibulomelic dysplasia"
      },
      {
        "code" : "2743",
        "display" : "Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome"
      },
      {
        "code" : "2744",
        "display" : "Horizontal gaze palsy with progressive scoliosis"
      },
      {
        "code" : "2745",
        "display" : "Opitz GBBB syndrome"
      },
      {
        "code" : "2746",
        "display" : "Opsismodysplasia"
      },
      {
        "code" : "275",
        "display" : "Severe combined immunodeficiency due to DCLRE1C deficiency"
      },
      {
        "code" : "2750",
        "display" : "Orofaciodigital syndrome type 1"
      },
      {
        "code" : "2751",
        "display" : "Orofaciodigital syndrome type 2"
      },
      {
        "code" : "2753",
        "display" : "Orofaciodigital syndrome type 4"
      },
      {
        "code" : "2754",
        "display" : "Orofaciodigital syndrome type 6"
      },
      {
        "code" : "2755",
        "display" : "Orofaciodigital syndrome type 8"
      },
      {
        "code" : "275517",
        "display" : "Autoimmune lymphoproliferative syndrome-recurrent viral infections due to CASP8 deficiency"
      },
      {
        "code" : "275523",
        "display" : "Dianzani autoimmune lymphoproliferative disease"
      },
      {
        "code" : "275543",
        "display" : "L1 syndrome"
      },
      {
        "code" : "275555",
        "display" : "Preeclampsia"
      },
      {
        "code" : "275761",
        "display" : "Lysosomal acid lipase deficiency"
      },
      {
        "code" : "275766",
        "display" : "Idiopathic pulmonary arterial hypertension"
      },
      {
        "code" : "275777",
        "display" : "Heritable pulmonary arterial hypertension"
      },
      {
        "code" : "275864",
        "display" : "Behavioral variant of frontotemporal dementia"
      },
      {
        "code" : "275872",
        "display" : "Frontotemporal dementia with motor neuron disease"
      },
      {
        "code" : "2759",
        "display" : "Imperforate oropharynx-costovertebral anomalies syndrome"
      },
      {
        "code" : "275944",
        "display" : "Hemolytic disease of the newborn with Kell alloimmunization"
      },
      {
        "code" : "276",
        "display" : "T-B+ severe combined immunodeficiency due to gamma chain deficiency"
      },
      {
        "code" : "2760",
        "display" : "OSLAM syndrome"
      },
      {
        "code" : "276066",
        "display" : "Bile acid CoA ligase deficiency and defective amidation"
      },
      {
        "code" : "276145",
        "display" : "Malignant epithelial tumor of salivary glands"
      },
      {
        "code" : "276148",
        "display" : "Benign epithelial tumor of salivary glands"
      },
      {
        "code" : "276152",
        "display" : "Multiple endocrine neoplasia type 4"
      },
      {
        "code" : "276174",
        "display" : "Idiopathic recurrent stupor"
      },
      {
        "code" : "276183",
        "display" : "Spinocerebellar ataxia type 32"
      },
      {
        "code" : "276193",
        "display" : "Spinocerebellar ataxia type 35"
      },
      {
        "code" : "276198",
        "display" : "Spinocerebellar ataxia type 36"
      },
      {
        "code" : "2762",
        "display" : "Progressive osseous heteroplasia"
      },
      {
        "code" : "276212",
        "display" : "Mucopolysaccharidosis type 6, rapidly progressing"
      },
      {
        "code" : "276223",
        "display" : "Mucopolysaccharidosis type 6, slowly progressing"
      },
      {
        "code" : "276234",
        "display" : "Non-syndromic male infertility due to sperm motility disorder"
      },
      {
        "code" : "276238",
        "display" : "Machado-Joseph disease type 1"
      },
      {
        "code" : "276241",
        "display" : "Machado-Joseph disease type 2"
      },
      {
        "code" : "276244",
        "display" : "Machado-Joseph disease type 3"
      },
      {
        "code" : "276280",
        "display" : "Hemihyperplasia-multiple lipomatosis syndrome"
      },
      {
        "code" : "2763",
        "display" : "Osteocraniostenosis"
      },
      {
        "code" : "276399",
        "display" : "Familial multinodular goiter"
      },
      {
        "code" : "2764",
        "display" : "Osteochondritis dissecans"
      },
      {
        "code" : "276405",
        "display" : "Hyperbiliverdinemia"
      },
      {
        "code" : "276413",
        "display" : "10q22.3q23.3 microdeletion syndrome"
      },
      {
        "code" : "276422",
        "display" : "10q22.3q23.3 microduplication syndrome"
      },
      {
        "code" : "276429",
        "display" : "Hypnic headache"
      },
      {
        "code" : "276432",
        "display" : "Ogden syndrome"
      },
      {
        "code" : "276435",
        "display" : "Lower motor neuron syndrome with late-adult onset"
      },
      {
        "code" : "276556",
        "display" : "Hyperinsulinism due to UCP2 deficiency"
      },
      {
        "code" : "276575",
        "display" : "Autosomal dominant hyperinsulinism due to SUR1 deficiency"
      },
      {
        "code" : "276580",
        "display" : "Autosomal dominant hyperinsulinism due to Kir6.2 deficiency"
      },
      {
        "code" : "276598",
        "display" : "Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency"
      },
      {
        "code" : "276603",
        "display" : "Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency"
      },
      {
        "code" : "276608",
        "display" : "Non-insulinoma pancreatogenous hypoglycemia syndrome"
      },
      {
        "code" : "276621",
        "display" : "Sporadic pheochromocytoma/secreting paraganglioma"
      },
      {
        "code" : "276630",
        "display" : "Symptomatic form of Coffin-Lowry syndrome in female carriers"
      },
      {
        "code" : "2767",
        "display" : "Carpotarsal osteochondromatosis"
      },
      {
        "code" : "2768",
        "display" : "Blount disease"
      },
      {
        "code" : "2769",
        "display" : "Familial osteodysplasia, Anderson type"
      },
      {
        "code" : "277",
        "display" : "Severe combined immunodeficiency due to adenosine deaminase deficiency"
      },
      {
        "code" : "2770",
        "display" : "Nasu-Hakola disease"
      },
      {
        "code" : "2771",
        "display" : "Bruck syndrome"
      },
      {
        "code" : "2772",
        "display" : "Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome"
      },
      {
        "code" : "2773",
        "display" : "Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome"
      },
      {
        "code" : "2774",
        "display" : "Multicentric carpo-tarsal osteolysis with or without nephropathy"
      },
      {
        "code" : "2776",
        "display" : "Autosomal recessive distal osteolysis syndrome"
      },
      {
        "code" : "2777",
        "display" : "Osteomesopyknosis"
      },
      {
        "code" : "2779",
        "display" : "Osteopathia striata-pigmentary dermopathy-white forelock syndrome"
      },
      {
        "code" : "2780",
        "display" : "Osteopathia striata-cranial sclerosis syndrome"
      },
      {
        "code" : "2783",
        "display" : "Autosomal dominant osteopetrosis type 1"
      },
      {
        "code" : "2785",
        "display" : "Osteopetrosis with renal tubular acidosis"
      },
      {
        "code" : "2786",
        "display" : "Osteoporosis-oculocutaneous hypopigmentation syndrome"
      },
      {
        "code" : "2788",
        "display" : "Osteoporosis-pseudoglioma syndrome"
      },
      {
        "code" : "2789",
        "display" : "Lateral meningocele syndrome"
      },
      {
        "code" : "2790",
        "display" : "Endosteal hyperostosis, Worth type"
      },
      {
        "code" : "2791",
        "display" : "Otodental syndrome"
      },
      {
        "code" : "2792",
        "display" : "Otofaciocervical syndrome"
      },
      {
        "code" : "2793",
        "display" : "Otoonychoperoneal syndrome"
      },
      {
        "code" : "2795",
        "display" : "Fowler urethral sphincter dysfunction syndrome"
      },
      {
        "code" : "2796",
        "display" : "Pachydermoperiostosis"
      },
      {
        "code" : "2798",
        "display" : "Pachygyria-intellectual disability-epilepsy syndrome"
      },
      {
        "code" : "279882",
        "display" : "Spasmus nutans"
      },
      {
        "code" : "279888",
        "display" : "Acute endophthalmitis"
      },
      {
        "code" : "279891",
        "display" : "Chronic endophthalmitis"
      },
      {
        "code" : "279894",
        "display" : "Toxic maculopathy due to antimalarial drugs"
      },
      {
        "code" : "279897",
        "display" : "Primary oculocerebral lymphoma"
      },
      {
        "code" : "279904",
        "display" : "Primary intraocular lymphoma"
      },
      {
        "code" : "279914",
        "display" : "Intermediate uveitis"
      },
      {
        "code" : "279919",
        "display" : "Infectious posterior uveitis"
      },
      {
        "code" : "279922",
        "display" : "Infectious anterior uveitis"
      },
      {
        "code" : "279925",
        "display" : "Infectious panuveitis"
      },
      {
        "code" : "279928",
        "display" : "Paraneoplastic uveitis"
      },
      {
        "code" : "279934",
        "display" : "Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency"
      },
      {
        "code" : "279943",
        "display" : "Hereditary neutrophilia"
      },
      {
        "code" : "279947",
        "display" : "Postorgasmic illness syndrome"
      },
      {
        "code" : "28",
        "display" : "Vitamin B12-responsive methylmalonic acidemia"
      },
      {
        "code" : "280",
        "display" : "Wolf-Hirschhorn syndrome"
      },
      {
        "code" : "2800",
        "display" : "Extramammary Paget disease"
      },
      {
        "code" : "280062",
        "display" : "Calciphylaxis"
      },
      {
        "code" : "280065",
        "display" : "Calciphylaxis cutis"
      },
      {
        "code" : "280068",
        "display" : "Visceral calciphylaxis"
      },
      {
        "code" : "280071",
        "display" : "ALG11-CDG"
      },
      {
        "code" : "2801",
        "display" : "Juvenile Paget disease"
      },
      {
        "code" : "280133",
        "display" : "Complement component 3 deficiency"
      },
      {
        "code" : "280142",
        "display" : "Severe combined immunodeficiency due to LCK deficiency"
      },
      {
        "code" : "280183",
        "display" : "Methylmalonic aciduria due to transcobalamin receptor defect"
      },
      {
        "code" : "280195",
        "display" : "Septopreoptic holoprosencephaly"
      },
      {
        "code" : "2802",
        "display" : "X-linked sideroblastic anemia and spinocerebellar ataxia"
      },
      {
        "code" : "280200",
        "display" : "Microform holoprosencephaly"
      },
      {
        "code" : "280205",
        "display" : "Laryngotracheoesophageal cleft type 0"
      },
      {
        "code" : "280210",
        "display" : "Pelizaeus-Merzbacher disease, connatal form"
      },
      {
        "code" : "280219",
        "display" : "Pelizaeus-Merzbacher disease, classic form"
      },
      {
        "code" : "280224",
        "display" : "Pelizaeus-Merzbacher disease, transitional form"
      },
      {
        "code" : "280229",
        "display" : "Pelizaeus-Merzbacher disease in female carriers"
      },
      {
        "code" : "280234",
        "display" : "Null syndrome"
      },
      {
        "code" : "280270",
        "display" : "Pelizaeus-Merzbacher-like disease"
      },
      {
        "code" : "280282",
        "display" : "Pelizaeus-Merzbacher-like disease due to GJC2 mutation"
      },
      {
        "code" : "280288",
        "display" : "Pelizaeus-Merzbacher-like disease due to HSPD1 mutation"
      },
      {
        "code" : "280293",
        "display" : "Pelizaeus-Merzbacher-like disease due to AIMP1 mutation"
      },
      {
        "code" : "280302",
        "display" : "Autoimmune pancreatitis type 1"
      },
      {
        "code" : "280315",
        "display" : "Autoimmune pancreatitis type 2"
      },
      {
        "code" : "280325",
        "display" : "Distal deletion 12p syndrome"
      },
      {
        "code" : "280333",
        "display" : "Alpha-dystroglycan-related limb-girdle muscular dystrophy R16"
      },
      {
        "code" : "280356",
        "display" : "PLIN1-related familial partial lipodystrophy"
      },
      {
        "code" : "280365",
        "display" : "Autosomal semi-dominant severe lipodystrophic laminopathy"
      },
      {
        "code" : "280379",
        "display" : "Erythropoietic uroporphyria associated with myeloid malignancy"
      },
      {
        "code" : "280384",
        "display" : "Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome"
      },
      {
        "code" : "280397",
        "display" : "Familial Alzheimer-like prion disease"
      },
      {
        "code" : "2804",
        "display" : "W syndrome"
      },
      {
        "code" : "280403",
        "display" : "Familial omphalocele syndrome with facial dysmorphism"
      },
      {
        "code" : "280406",
        "display" : "Familial steroid-resistant nephrotic syndrome with sensorineural deafness"
      },
      {
        "code" : "2805",
        "display" : "Partial pancreatic agenesis"
      },
      {
        "code" : "280553",
        "display" : "Fatal infantile hypertonic myofibrillar myopathy"
      },
      {
        "code" : "280558",
        "display" : "Warsaw breakage syndrome"
      },
      {
        "code" : "280576",
        "display" : "Nestor-Guillermo progeria syndrome"
      },
      {
        "code" : "280586",
        "display" : "Chondrodysplasia with joint dislocations, gPAPP type"
      },
      {
        "code" : "280598",
        "display" : "Hereditary sensorimotor neuropathy with hyperelastic skin"
      },
      {
        "code" : "2806",
        "display" : "Subacute sclerosing leukoencephalitis"
      },
      {
        "code" : "280615",
        "display" : "Hemoglobinopathy Toms River"
      },
      {
        "code" : "280620",
        "display" : "Progressive myoclonic epilepsy type 6"
      },
      {
        "code" : "280628",
        "display" : "Familial progressive hyper- and hypopigmentation"
      },
      {
        "code" : "280633",
        "display" : "Multiple congenital anomalies-hypotonia-seizures syndrome"
      },
      {
        "code" : "280640",
        "display" : "Occipital pachygyria and polymicrogyria"
      },
      {
        "code" : "280654",
        "display" : "Autosomal recessive nail dysplasia"
      },
      {
        "code" : "280671",
        "display" : "Megaconial congenital muscular dystrophy"
      },
      {
        "code" : "280679",
        "display" : "Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome"
      },
      {
        "code" : "2807",
        "display" : "Papilloma of choroid plexus"
      },
      {
        "code" : "280763",
        "display" : "Severe intellectual disability and progressive spastic paraplegia"
      },
      {
        "code" : "280774",
        "display" : "Generalized essential telangiectasia"
      },
      {
        "code" : "280779",
        "display" : "Cutaneous collagenous vasculopathy"
      },
      {
        "code" : "280785",
        "display" : "Bullous diffuse cutaneous mastocytosis"
      },
      {
        "code" : "280794",
        "display" : "Pseudoxanthomatous diffuse cutaneous mastocytosis"
      },
      {
        "code" : "2808",
        "display" : "Laryngeal abductor paralysis"
      },
      {
        "code" : "280802",
        "display" : "Intralobar congenital pulmonary sequestration"
      },
      {
        "code" : "280811",
        "display" : "Extralobar congenital pulmonary sequestration"
      },
      {
        "code" : "280821",
        "display" : "Communicating congenital bronchopulmonary-foregut malformation"
      },
      {
        "code" : "280827",
        "display" : "Congenital pulmonary airway malformation type 0"
      },
      {
        "code" : "280832",
        "display" : "Congenital pulmonary airway malformation type 1"
      },
      {
        "code" : "280840",
        "display" : "Congenital pulmonary airway malformation type 2"
      },
      {
        "code" : "280847",
        "display" : "Congenital pulmonary airway malformation type 3"
      },
      {
        "code" : "280854",
        "display" : "Congenital pulmonary airway malformation type 4"
      },
      {
        "code" : "2809",
        "display" : "Familial recurrent peripheral facial palsy"
      },
      {
        "code" : "280914",
        "display" : "Isolated idiopathic anterior uveitis"
      },
      {
        "code" : "280917",
        "display" : "Idiopathic posterior uveitis"
      },
      {
        "code" : "280921",
        "display" : "Idiopathic panuveitis"
      },
      {
        "code" : "281",
        "display" : "Monosomy 5p syndrome"
      },
      {
        "code" : "281090",
        "display" : "Syndromic recessive X-linked ichthyosis"
      },
      {
        "code" : "281122",
        "display" : "Self-improving collodion baby"
      },
      {
        "code" : "281127",
        "display" : "Acral self-healing collodion baby"
      },
      {
        "code" : "281139",
        "display" : "Annular epidermolytic ichthyosis"
      },
      {
        "code" : "281190",
        "display" : "Congenital reticular ichthyosiform erythroderma"
      },
      {
        "code" : "2812",
        "display" : "Parana hard skin syndrome"
      },
      {
        "code" : "281201",
        "display" : "Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome"
      },
      {
        "code" : "2815",
        "display" : "Spastic paraparesis-deafness syndrome"
      },
      {
        "code" : "2818",
        "display" : "Spastic paraplegia-glaucoma-intellectual disability syndrome"
      },
      {
        "code" : "2819",
        "display" : "Spastic paraplegia-facial-cutaneous lesions syndrome"
      },
      {
        "code" : "2820",
        "display" : "Spastic paraplegia-nephritis-deafness syndrome"
      },
      {
        "code" : "2821",
        "display" : "Spastic paraplegia-neuropathy-poikiloderma syndrome"
      },
      {
        "code" : "282166",
        "display" : "Inherited Creutzfeldt-Jakob disease"
      },
      {
        "code" : "2822",
        "display" : "Autosomal recessive spastic paraplegia type 11"
      },
      {
        "code" : "2824",
        "display" : "Paraplegia-intellectual disability-hyperkeratosis syndrome"
      },
      {
        "code" : "2825",
        "display" : "PARC syndrome"
      },
      {
        "code" : "2826",
        "display" : "Spastic paraplegia-precocious puberty syndrome"
      },
      {
        "code" : "2828",
        "display" : "Young-onset Parkinson disease"
      },
      {
        "code" : "283",
        "display" : "Demodicidosis"
      },
      {
        "code" : "2831",
        "display" : "Rhizomelic dysplasia, Patterson-Lowry type"
      },
      {
        "code" : "2832",
        "display" : "Short tarsus-absence of lower eyelashes syndrome"
      },
      {
        "code" : "2833",
        "display" : "Stiff skin syndrome"
      },
      {
        "code" : "2834",
        "display" : "Wrinkly skin syndrome"
      },
      {
        "code" : "2835",
        "display" : "Pectus excavatum-macrocephaly-dysplastic nails syndrome"
      },
      {
        "code" : "2836",
        "display" : "PEHO syndrome"
      },
      {
        "code" : "28378",
        "display" : "Tyrosinemia type 2"
      },
      {
        "code" : "2838",
        "display" : "Renal caliceal diverticuli-deafness syndrome"
      },
      {
        "code" : "2839",
        "display" : "Pelvis-shoulder dysplasia"
      },
      {
        "code" : "284",
        "display" : "Alveolar echinococcosis"
      },
      {
        "code" : "2840",
        "display" : "Pelvic dysplasia-arthrogryposis of lower limbs syndrome"
      },
      {
        "code" : "2841",
        "display" : "Hailey-Hailey disease"
      },
      {
        "code" : "284139",
        "display" : "Larsen-like syndrome, B3GAT3 type"
      },
      {
        "code" : "284149",
        "display" : "Craniosynostosis-dental anomalies"
      },
      {
        "code" : "284160",
        "display" : "8q21.11 microdeletion syndrome"
      },
      {
        "code" : "284169",
        "display" : "Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion"
      },
      {
        "code" : "284180",
        "display" : "Xp22.13p22.2 duplication syndrome"
      },
      {
        "code" : "2842",
        "display" : "Penoscrotal transposition"
      },
      {
        "code" : "284227",
        "display" : "TEMPI syndrome"
      },
      {
        "code" : "284232",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2O"
      },
      {
        "code" : "284247",
        "display" : "Familial retinal arterial macroaneurysm"
      },
      {
        "code" : "284271",
        "display" : "Autosomal recessive cerebellar ataxia-psychomotor delay syndrome"
      },
      {
        "code" : "284282",
        "display" : "Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency"
      },
      {
        "code" : "284289",
        "display" : "Adult-onset autosomal recessive cerebellar ataxia"
      },
      {
        "code" : "2843",
        "display" : "Pentosuria"
      },
      {
        "code" : "284324",
        "display" : "Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia"
      },
      {
        "code" : "284332",
        "display" : "Infantile-onset autosomal recessive nonprogressive cerebellar ataxia"
      },
      {
        "code" : "284339",
        "display" : "Pontocerebellar hypoplasia type 7"
      },
      {
        "code" : "284343",
        "display" : "DICER1 tumor-predisposition syndrome"
      },
      {
        "code" : "284362",
        "display" : "Fetal lung interstitial tumor"
      },
      {
        "code" : "284388",
        "display" : "Reversible cerebral vasoconstriction syndrome"
      },
      {
        "code" : "284395",
        "display" : "Well-differentiated fetal adenocarcinoma of the lung"
      },
      {
        "code" : "284400",
        "display" : "Small cell carcinoma of the bladder"
      },
      {
        "code" : "284411",
        "display" : "Glycerol kinase deficiency, juvenile form"
      },
      {
        "code" : "284414",
        "display" : "Glycerol kinase deficiency, adult form"
      },
      {
        "code" : "284417",
        "display" : "Phosphoserine aminotransferase deficiency, infantile/juvenile form"
      },
      {
        "code" : "284426",
        "display" : "Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency"
      },
      {
        "code" : "284435",
        "display" : "Glycogen storage disease due to lactate dehydrogenase H-subunit deficiency"
      },
      {
        "code" : "284448",
        "display" : "CLIPPERS"
      },
      {
        "code" : "284454",
        "display" : "Acute zonal occult outer retinopathy"
      },
      {
        "code" : "284460",
        "display" : "Acute annular outer retinopathy"
      },
      {
        "code" : "2847",
        "display" : "Pericardial and diaphragmatic defect"
      },
      {
        "code" : "2848",
        "display" : "Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome"
      },
      {
        "code" : "2849",
        "display" : "Perlman syndrome"
      },
      {
        "code" : "284963",
        "display" : "Marfan syndrome type 1"
      },
      {
        "code" : "284973",
        "display" : "Marfan syndrome type 2"
      },
      {
        "code" : "284979",
        "display" : "Neonatal Marfan syndrome"
      },
      {
        "code" : "284984",
        "display" : "Aneurysm-osteoarthritis syndrome"
      },
      {
        "code" : "285",
        "display" : "Hypermobile Ehlers-Danlos syndrome"
      },
      {
        "code" : "2850",
        "display" : "Alopecia-intellectual disability syndrome"
      },
      {
        "code" : "2854",
        "display" : "Fuhrmann syndrome"
      },
      {
        "code" : "2855",
        "display" : "Perrault syndrome"
      },
      {
        "code" : "2856",
        "display" : "Persistent Müllerian duct syndrome"
      },
      {
        "code" : "286",
        "display" : "Vascular Ehlers-Danlos syndrome"
      },
      {
        "code" : "2863",
        "display" : "Short stature-wormian bones-dextrocardia syndrome"
      },
      {
        "code" : "2865",
        "display" : "Short stature-webbed neck-heart disease syndrome"
      },
      {
        "code" : "2866",
        "display" : "Short stature-deafness-neutrophil dysfunction-dysmorphism syndrome"
      },
      {
        "code" : "2867",
        "display" : "Short stature, Brussels type"
      },
      {
        "code" : "2868",
        "display" : "Short stature-valvular heart disease-characteristic facies syndrome"
      },
      {
        "code" : "2869",
        "display" : "Peutz-Jeghers syndrome"
      },
      {
        "code" : "287",
        "display" : "Classical Ehlers-Danlos syndrome"
      },
      {
        "code" : "2871",
        "display" : "Pfeiffer-Palm-Teller syndrome"
      },
      {
        "code" : "2872",
        "display" : "Cardiocranial syndrome, Pfeiffer type"
      },
      {
        "code" : "2874",
        "display" : "Phakomatosis pigmentokeratotica"
      },
      {
        "code" : "2875",
        "display" : "Phakomatosis pigmentovascularis"
      },
      {
        "code" : "2876",
        "display" : "PHAVER syndrome"
      },
      {
        "code" : "2879",
        "display" : "Phocomelia, Schinzel type"
      },
      {
        "code" : "288",
        "display" : "Hereditary elliptocytosis"
      },
      {
        "code" : "2880",
        "display" : "Phosphoenolpyruvate carboxykinase deficiency"
      },
      {
        "code" : "2881",
        "display" : "Cutaneous photosensitivity-lethal colitis syndrome"
      },
      {
        "code" : "2882",
        "display" : "Sitosterolemia"
      },
      {
        "code" : "2884",
        "display" : "Piebaldism"
      },
      {
        "code" : "2885",
        "display" : "Piebald trait-neurologic defects syndrome"
      },
      {
        "code" : "2886",
        "display" : "TARP syndrome"
      },
      {
        "code" : "2888",
        "display" : "Pierre Robin syndrome-faciodigital anomaly syndrome"
      },
      {
        "code" : "2889",
        "display" : "Pili torti"
      },
      {
        "code" : "289",
        "display" : "Ellis Van Creveld syndrome"
      },
      {
        "code" : "2890",
        "display" : "Pili torti-onychodysplasia syndrome"
      },
      {
        "code" : "2891",
        "display" : "Pili torti-developmental delay-neurological abnormalities syndrome"
      },
      {
        "code" : "289157",
        "display" : "Hypocalcemic vitamin D-dependent rickets"
      },
      {
        "code" : "289176",
        "display" : "Autosomal recessive hypophosphatemic rickets"
      },
      {
        "code" : "2892",
        "display" : "Pilodental dysplasia-refractive errors syndrome"
      },
      {
        "code" : "289266",
        "display" : "Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation"
      },
      {
        "code" : "289290",
        "display" : "Hypermethioninemia encephalopathy due to adenosine kinase deficiency"
      },
      {
        "code" : "289307",
        "display" : "Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency"
      },
      {
        "code" : "289326",
        "display" : "Tropical spastic paraparesis"
      },
      {
        "code" : "289347",
        "display" : "Infective dermatitis associated with HTLV-1"
      },
      {
        "code" : "289356",
        "display" : "Primary non-gestational choriocarcinoma of ovary"
      },
      {
        "code" : "289362",
        "display" : "Non-central nervous system-localized embryonal carcinoma"
      },
      {
        "code" : "289365",
        "display" : "Familial vesicoureteral reflux"
      },
      {
        "code" : "289377",
        "display" : "Early-onset myopathy with fatal cardiomyopathy"
      },
      {
        "code" : "289380",
        "display" : "Myosclerosis"
      },
      {
        "code" : "289385",
        "display" : "Malignancy diagnosed during pregnancy"
      },
      {
        "code" : "289390",
        "display" : "Primary Sjögren disease"
      },
      {
        "code" : "289465",
        "display" : "Isolated congenital adermatoglyphia"
      },
      {
        "code" : "289478",
        "display" : "PASH syndrome"
      },
      {
        "code" : "289483",
        "display" : "Intellectual disability-alacrima-achalasia syndrome"
      },
      {
        "code" : "289494",
        "display" : "4H leukodystrophy"
      },
      {
        "code" : "289499",
        "display" : "Congenital cataract microcornea with corneal opacity"
      },
      {
        "code" : "289504",
        "display" : "Combined malonic and methylmalonic acidemia"
      },
      {
        "code" : "289513",
        "display" : "12q15q21 microdeletion syndrome"
      },
      {
        "code" : "289522",
        "display" : "Microtriplication 11q24.1 syndrome"
      },
      {
        "code" : "289539",
        "display" : "BAP1-related tumor predisposition syndrome"
      },
      {
        "code" : "289548",
        "display" : "Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency"
      },
      {
        "code" : "289553",
        "display" : "Dysmorphism-conductive hearing loss-heart defect syndrome"
      },
      {
        "code" : "289560",
        "display" : "Mitochondrial membrane protein-associated neurodegeneration"
      },
      {
        "code" : "289586",
        "display" : "Exfoliative ichthyosis"
      },
      {
        "code" : "289596",
        "display" : "Juvenile nasopharyngeal angiofibroma"
      },
      {
        "code" : "2896",
        "display" : "Pitt-Hopkins syndrome"
      },
      {
        "code" : "289601",
        "display" : "Hereditary arterial and articular multiple calcification syndrome"
      },
      {
        "code" : "289661",
        "display" : "Epstein-Barr virus-positive diffuse large B-cell lymphoma"
      },
      {
        "code" : "289666",
        "display" : "Plasmablastic lymphoma"
      },
      {
        "code" : "289682",
        "display" : "Lymphoepithelial-like carcinoma"
      },
      {
        "code" : "289685",
        "display" : "Myopericytoma"
      },
      {
        "code" : "2897",
        "display" : "Pityriasis rubra pilaris"
      },
      {
        "code" : "2898",
        "display" : "X-linked intellectual disability-plagiocephaly syndrome"
      },
      {
        "code" : "289846",
        "display" : "Glutathione synthetase deficiency with 5-oxoprolinuria"
      },
      {
        "code" : "289849",
        "display" : "Glutathione synthetase deficiency without 5-oxoprolinuria"
      },
      {
        "code" : "289857",
        "display" : "Neonatal glycine encephalopathy"
      },
      {
        "code" : "289860",
        "display" : "Infantile glycine encephalopathy"
      },
      {
        "code" : "289863",
        "display" : "Atypical glycine encephalopathy"
      },
      {
        "code" : "289877",
        "display" : "Transient hyperammonemia of the newborn"
      },
      {
        "code" : "289891",
        "display" : "Hypermethioninemia due to glycine N-methyltransferase deficiency"
      },
      {
        "code" : "2899",
        "display" : "Brachyolmia-amelogenesis imperfecta syndrome"
      },
      {
        "code" : "289916",
        "display" : "Vitamin B12-unresponsive methylmalonic acidemia type mut0"
      },
      {
        "code" : "29",
        "display" : "Mevalonic aciduria"
      },
      {
        "code" : "290",
        "display" : "Congenital rubella syndrome"
      },
      {
        "code" : "2900",
        "display" : "Leri pleonosteosis"
      },
      {
        "code" : "2901",
        "display" : "Neuralgic amyotrophy"
      },
      {
        "code" : "2902",
        "display" : "Idiopathic chronic eosinophilic pneumonia"
      },
      {
        "code" : "2903",
        "display" : "Familial spontaneous pneumothorax"
      },
      {
        "code" : "2905",
        "display" : "POEMS syndrome"
      },
      {
        "code" : "2907",
        "display" : "Hereditary acrokeratotic poikiloderma"
      },
      {
        "code" : "29072",
        "display" : "Hereditary pheochromocytoma-paraganglioma"
      },
      {
        "code" : "29073",
        "display" : "Multiple myeloma"
      },
      {
        "code" : "2908",
        "display" : "Kindler epidermolysis bullosa"
      },
      {
        "code" : "2909",
        "display" : "Rothmund-Thomson syndrome"
      },
      {
        "code" : "291",
        "display" : "Congenital varicella syndrome"
      },
      {
        "code" : "2911",
        "display" : "Poland syndrome"
      },
      {
        "code" : "2912",
        "display" : "Poliomyelitis"
      },
      {
        "code" : "2916",
        "display" : "Postaxial polydactyly-dental and vertebral anomalies syndrome"
      },
      {
        "code" : "2917",
        "display" : "Polydactyly-myopia syndrome"
      },
      {
        "code" : "2919",
        "display" : "Orofaciodigital syndrome type 5"
      },
      {
        "code" : "292",
        "display" : "Congenital enterovirus infection"
      },
      {
        "code" : "2920",
        "display" : "Oliver syndrome"
      },
      {
        "code" : "29207",
        "display" : "Reactive arthritis"
      },
      {
        "code" : "2921",
        "display" : "Preaxial polydactyly-colobomata-intellectual disability syndrome"
      },
      {
        "code" : "2924",
        "display" : "Isolated polycystic liver disease"
      },
      {
        "code" : "2926",
        "display" : "Digital extensor muscle aplasia-polyneuropathy"
      },
      {
        "code" : "2928",
        "display" : "Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome"
      },
      {
        "code" : "2929",
        "display" : "Juvenile polyposis syndrome"
      },
      {
        "code" : "293",
        "display" : "Congenital herpes simplex virus infection"
      },
      {
        "code" : "2930",
        "display" : "Cronkhite-Canada syndrome"
      },
      {
        "code" : "293144",
        "display" : "Familial clubfoot due to 5q31 microdeletion"
      },
      {
        "code" : "293150",
        "display" : "Familial clubfoot due to PITX1 point mutation"
      },
      {
        "code" : "293165",
        "display" : "Skin fragility-woolly hair-palmoplantar keratoderma syndrome"
      },
      {
        "code" : "293168",
        "display" : "Infantile-onset ascending hereditary spastic paralysis"
      },
      {
        "code" : "293173",
        "display" : "Acute generalized exanthematous pustulosis"
      },
      {
        "code" : "293181",
        "display" : "Epilepsy of infancy with migrating focal seizures"
      },
      {
        "code" : "293199",
        "display" : "Pleomorphic rhabdomyosarcoma"
      },
      {
        "code" : "2932",
        "display" : "Chronic inflammatory demyelinating polyneuropathy"
      },
      {
        "code" : "293202",
        "display" : "Epithelioid sarcoma"
      },
      {
        "code" : "293208",
        "display" : "Celiac artery compression syndrome"
      },
      {
        "code" : "293284",
        "display" : "Tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria"
      },
      {
        "code" : "293375",
        "display" : "Grayson-Wilbrandt corneal dystrophy"
      },
      {
        "code" : "293381",
        "display" : "Epithelial recurrent erosion dystrophy"
      },
      {
        "code" : "2934",
        "display" : "Polysyndactyly-cardiac malformation syndrome"
      },
      {
        "code" : "293462",
        "display" : "Pre-Descemet corneal dystrophy"
      },
      {
        "code" : "2935",
        "display" : "Crossed polysyndactyly"
      },
      {
        "code" : "293603",
        "display" : "Congenital hereditary endothelial dystrophy type II"
      },
      {
        "code" : "293621",
        "display" : "X-linked endothelial corneal dystrophy"
      },
      {
        "code" : "293633",
        "display" : "PYCR1-related De Barsy syndrome"
      },
      {
        "code" : "293707",
        "display" : "Blepharophimosis-intellectual disability syndrome, MKB type"
      },
      {
        "code" : "293725",
        "display" : "Blepharophimosis-intellectual disability syndrome, Verloes type"
      },
      {
        "code" : "293807",
        "display" : "Ketamine-induced biliary dilatation"
      },
      {
        "code" : "293812",
        "display" : "Fixed drug eruption"
      },
      {
        "code" : "293822",
        "display" : "MITF-related melanoma and renal cell carcinoma predisposition syndrome"
      },
      {
        "code" : "293825",
        "display" : "Congenital dyserythropoietic anemia type IV"
      },
      {
        "code" : "293843",
        "display" : "3MC syndrome"
      },
      {
        "code" : "293864",
        "display" : "Hypoplastic pancreas-intestinal atresia-hypoplastic gallbladder syndrome"
      },
      {
        "code" : "293888",
        "display" : "Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variant"
      },
      {
        "code" : "293899",
        "display" : "Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variant"
      },
      {
        "code" : "293910",
        "display" : "Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variant"
      },
      {
        "code" : "293925",
        "display" : "Lethal occipital encephalocele-skeletal dysplasia syndrome"
      },
      {
        "code" : "293936",
        "display" : "EDICT syndrome"
      },
      {
        "code" : "293939",
        "display" : "Distal Xq28 microduplication syndrome"
      },
      {
        "code" : "293948",
        "display" : "1p21.3 microdeletion syndrome"
      },
      {
        "code" : "293955",
        "display" : "Childhood encephalopathy due to thiamine pyrophosphokinase deficiency"
      },
      {
        "code" : "293958",
        "display" : "Hypertelorism-preauricular sinus-punctual pits-deafness syndrome"
      },
      {
        "code" : "293964",
        "display" : "Hypoinsulinemic hypoglycemia and body hemihypertrophy"
      },
      {
        "code" : "293967",
        "display" : "Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome"
      },
      {
        "code" : "293978",
        "display" : "Deficiency in anterior pituitary function-variable immunodeficiency syndrome"
      },
      {
        "code" : "293987",
        "display" : "Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome"
      },
      {
        "code" : "294",
        "display" : "Fetal cytomegalovirus syndrome"
      },
      {
        "code" : "2940",
        "display" : "Porencephaly"
      },
      {
        "code" : "294016",
        "display" : "Microcephaly-capillary malformation syndrome"
      },
      {
        "code" : "294023",
        "display" : "Neonatal inflammatory skin and bowel disease"
      },
      {
        "code" : "294026",
        "display" : "Syndactyly-nystagmus syndrome due to 2q31.1 microduplication"
      },
      {
        "code" : "2941",
        "display" : "Porencephaly-cerebellar hypoplasia-internal malformations syndrome"
      },
      {
        "code" : "2942",
        "display" : "Postpoliomyelitis syndrome"
      },
      {
        "code" : "294415",
        "display" : "Renal-hepatic-pancreatic dysplasia"
      },
      {
        "code" : "294422",
        "display" : "Chronic intestinal failure"
      },
      {
        "code" : "2946",
        "display" : "Brachydactyly-long thumb syndrome"
      },
      {
        "code" : "2947",
        "display" : "Triphalangeal thumbs-brachyectrodactyly syndrome"
      },
      {
        "code" : "294967",
        "display" : "Isolated amelia of upper limb"
      },
      {
        "code" : "294969",
        "display" : "Isolated amelia of lower limb"
      },
      {
        "code" : "294971",
        "display" : "Isolated tetra-amelia"
      },
      {
        "code" : "294973",
        "display" : "Isolated humeral agenesis/hypoplasia"
      },
      {
        "code" : "294975",
        "display" : "Isolated absence of upper arm and forearm with hand present"
      },
      {
        "code" : "294977",
        "display" : "Isolated absence of thigh and lower leg with foot present"
      },
      {
        "code" : "294979",
        "display" : "Isolated absence of both forearm and hand"
      },
      {
        "code" : "294981",
        "display" : "Isolated absence of both lower leg and foot"
      },
      {
        "code" : "294983",
        "display" : "Isolated acheiria"
      },
      {
        "code" : "294986",
        "display" : "Isolated apodia"
      },
      {
        "code" : "294988",
        "display" : "Isolated hypoplasia of thumb"
      },
      {
        "code" : "295",
        "display" : "Fetal parvovirus syndrome"
      },
      {
        "code" : "295000",
        "display" : "Amniotic band syndrome"
      },
      {
        "code" : "295002",
        "display" : "Isolated hyperphalangy"
      },
      {
        "code" : "295004",
        "display" : "Central polydactyly"
      },
      {
        "code" : "295012",
        "display" : "Syndactyly type 6"
      },
      {
        "code" : "295014",
        "display" : "Familial isolated clinodactyly of fingers"
      },
      {
        "code" : "295016",
        "display" : "Camptodactyly of fingers"
      },
      {
        "code" : "295018",
        "display" : "Congenital pseudoarthrosis of the tibia"
      },
      {
        "code" : "295020",
        "display" : "Congenital pseudoarthrosis of the femur"
      },
      {
        "code" : "295022",
        "display" : "Congenital pseudoarthrosis of the fibula"
      },
      {
        "code" : "295024",
        "display" : "Congenital pseudoarthrosis of the radius"
      },
      {
        "code" : "295026",
        "display" : "Congenital pseudoarthrosis of the ulna"
      },
      {
        "code" : "295028",
        "display" : "Isolated tibio-fibular synostosis"
      },
      {
        "code" : "295030",
        "display" : "True congenital shoulder dislocation"
      },
      {
        "code" : "295032",
        "display" : "Isolated congenital radial head dislocation"
      },
      {
        "code" : "295034",
        "display" : "Congenital knee dislocation"
      },
      {
        "code" : "295036",
        "display" : "Congenital patella dislocation"
      },
      {
        "code" : "295044",
        "display" : "Macrodactyly of fingers"
      },
      {
        "code" : "295047",
        "display" : "Macrodactyly of toes"
      },
      {
        "code" : "295049",
        "display" : "Upper limb hypertrophy"
      },
      {
        "code" : "295051",
        "display" : "Lower limb hypertrophy"
      },
      {
        "code" : "2951",
        "display" : "Absent thumb-short stature-immunodeficiency syndrome"
      },
      {
        "code" : "295187",
        "display" : "Zygodactyly type 1"
      },
      {
        "code" : "295189",
        "display" : "Zygodactyly type 2"
      },
      {
        "code" : "295191",
        "display" : "Zygodactyly type 3"
      },
      {
        "code" : "295193",
        "display" : "Zygodactyly type 4"
      },
      {
        "code" : "295195",
        "display" : "Synpolydactyly type 1"
      },
      {
        "code" : "295197",
        "display" : "Synpolydactyly type 2"
      },
      {
        "code" : "295199",
        "display" : "Synpolydactyly type 3"
      },
      {
        "code" : "2952",
        "display" : "Adducted thumbs-arthrogryposis syndrome, Christian type"
      },
      {
        "code" : "295201",
        "display" : "Congenital vertical talus, unilateral"
      },
      {
        "code" : "295203",
        "display" : "Congenital vertical talus, bilateral"
      },
      {
        "code" : "295225",
        "display" : "Congenital elbow dislocation, unilateral"
      },
      {
        "code" : "295227",
        "display" : "Congenital elbow dislocation, bilateral"
      },
      {
        "code" : "295229",
        "display" : "Congenital genu recurvatum"
      },
      {
        "code" : "295232",
        "display" : "Congenital genu flexum"
      },
      {
        "code" : "295239",
        "display" : "Macrodactyly of fingers, unilateral"
      },
      {
        "code" : "295241",
        "display" : "Macrodactyly of fingers, bilateral"
      },
      {
        "code" : "295243",
        "display" : "Macrodactyly of toes, unilateral"
      },
      {
        "code" : "295245",
        "display" : "Macrodactyly of toes, bilateral"
      },
      {
        "code" : "2953",
        "display" : "Musculocontractural Ehlers-Danlos syndrome"
      },
      {
        "code" : "2956",
        "display" : "Acrodysplasia scoliosis"
      },
      {
        "code" : "2957",
        "display" : "Guttmacher syndrome"
      },
      {
        "code" : "2958",
        "display" : "X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome"
      },
      {
        "code" : "2959",
        "display" : "Progeria-short stature-pigmented nevi syndrome"
      },
      {
        "code" : "296",
        "display" : "Ollier disease"
      },
      {
        "code" : "2962",
        "display" : "De Barsy syndrome"
      },
      {
        "code" : "2963",
        "display" : "Progeroid syndrome, Petty type"
      },
      {
        "code" : "2964",
        "display" : "Autosomal dominant prognathism"
      },
      {
        "code" : "2965",
        "display" : "Prolactinoma"
      },
      {
        "code" : "2966",
        "display" : "Properdin deficiency"
      },
      {
        "code" : "2967",
        "display" : "Transcobalamin I deficiency"
      },
      {
        "code" : "2968",
        "display" : "Leukocyte adhesion deficiency"
      },
      {
        "code" : "2969",
        "display" : "Proteus-like syndrome"
      },
      {
        "code" : "297",
        "display" : "Tick-borne encephalitis"
      },
      {
        "code" : "2970",
        "display" : "Prune belly syndrome"
      },
      {
        "code" : "2971",
        "display" : "Peroxisomal acyl-CoA oxidase deficiency"
      },
      {
        "code" : "2972",
        "display" : "Non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome"
      },
      {
        "code" : "2973",
        "display" : "46,XX difference of sex development-anorectal anomalies syndrome"
      },
      {
        "code" : "2975",
        "display" : "46,XX difference of sex development-skeletal anomalies syndrome"
      },
      {
        "code" : "2976",
        "display" : "Pseudoleprechaunism syndrome, Patterson type"
      },
      {
        "code" : "2978",
        "display" : "Chronic intestinal pseudoobstruction syndrome"
      },
      {
        "code" : "298",
        "display" : "Mitochondrial neurogastrointestinal encephalomyopathy"
      },
      {
        "code" : "2980",
        "display" : "Acrootoocular syndrome"
      },
      {
        "code" : "29822",
        "display" : "Spontaneous periodic hypothermia"
      },
      {
        "code" : "2983",
        "display" : "Difference of sex development-intellectual disability syndrome"
      },
      {
        "code" : "2985",
        "display" : "Pseudoprogeria syndrome"
      },
      {
        "code" : "2987",
        "display" : "Antecubital pterygium syndrome"
      },
      {
        "code" : "2988",
        "display" : "Pterygium colli-intellectual disability-digital anomalies syndrome"
      },
      {
        "code" : "2989",
        "display" : "Familial pterygium of the conjunctiva"
      },
      {
        "code" : "2990",
        "display" : "Autosomal recessive multiple pterygium syndrome"
      },
      {
        "code" : "2994",
        "display" : "Short stature-craniofacial anomalies-genital hypoplasia syndrome"
      },
      {
        "code" : "2995",
        "display" : "Baraitser-Winter cerebrofrontofacial syndrome"
      },
      {
        "code" : "2997",
        "display" : "Ptosis-vocal cord paralysis syndrome"
      },
      {
        "code" : "2999",
        "display" : "Ptosis-strabismus-ectopic pupils syndrome"
      },
      {
        "code" : "30",
        "display" : "Hereditary orotic aciduria"
      },
      {
        "code" : "300",
        "display" : "Bifunctional enzyme deficiency"
      },
      {
        "code" : "3000",
        "display" : "Familial peripheral male-limited precocious puberty"
      },
      {
        "code" : "300179",
        "display" : "Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency"
      },
      {
        "code" : "3002",
        "display" : "Immune thrombocytopenia"
      },
      {
        "code" : "300284",
        "display" : "Connective tissue disorder due to lysyl hydroxylase-3 deficiency"
      },
      {
        "code" : "300293",
        "display" : "Transient infantile hypertriglyceridemia and hepatosteatosis"
      },
      {
        "code" : "300298",
        "display" : "Severe congenital hypochromic anemia with ringed sideroblasts"
      },
      {
        "code" : "3003",
        "display" : "Pyknoachondrogenesis"
      },
      {
        "code" : "300305",
        "display" : "11p15.4 microduplication syndrome"
      },
      {
        "code" : "300313",
        "display" : "Congenital cataract-hearing loss-severe developmental delay syndrome"
      },
      {
        "code" : "300319",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2P"
      },
      {
        "code" : "300324",
        "display" : "Persistent polyclonal B-cell lymphocytosis"
      },
      {
        "code" : "300333",
        "display" : "Nephrotic syndrome-epidermolysis bullosa-sensorineural deafness syndrome"
      },
      {
        "code" : "300345",
        "display" : "Autosomal systemic lupus erythematosus"
      },
      {
        "code" : "300359",
        "display" : "PLCG2-associated antibody deficiency and immune dysregulation"
      },
      {
        "code" : "300373",
        "display" : "X-linked acrogigantism"
      },
      {
        "code" : "300382",
        "display" : "Progeroid and marfanoid aspect-lipodystrophy syndrome"
      },
      {
        "code" : "300385",
        "display" : "Pituitary carcinoma"
      },
      {
        "code" : "3004",
        "display" : "Mirror polydactyly-vertebral segmentation-limbs defects syndrome"
      },
      {
        "code" : "300493",
        "display" : "Sagliker syndrome"
      },
      {
        "code" : "300496",
        "display" : "Multiple congenital anomalies-hypotonia-seizures syndrome type 2"
      },
      {
        "code" : "3005",
        "display" : "Pyle disease"
      },
      {
        "code" : "300501",
        "display" : "Painful orbital and systemic neurofibromas-marfanoid habitus syndrome"
      },
      {
        "code" : "300504",
        "display" : "Onychocytic matricoma"
      },
      {
        "code" : "300512",
        "display" : "Onychomatricoma"
      },
      {
        "code" : "300525",
        "display" : "Pseudohypoaldosteronism type 2D"
      },
      {
        "code" : "300530",
        "display" : "Pseudohypoaldosteronism type 2E"
      },
      {
        "code" : "300536",
        "display" : "DDOST-CDG"
      },
      {
        "code" : "300547",
        "display" : "Autosomal recessive infantile hypercalcemia"
      },
      {
        "code" : "300552",
        "display" : "Follicular cholangitis and pancreatitis"
      },
      {
        "code" : "300557",
        "display" : "Carcinoma of the ampulla of Vater"
      },
      {
        "code" : "300564",
        "display" : "Combined pulmonary fibrosis-emphysema syndrome"
      },
      {
        "code" : "300570",
        "display" : "Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation"
      },
      {
        "code" : "300573",
        "display" : "Polymicrogyria due to TUBB2B mutation"
      },
      {
        "code" : "3006",
        "display" : "Pyridoxine-dependent-developmental and epileptic encephalopathy"
      },
      {
        "code" : "300605",
        "display" : "Juvenile amyotrophic lateral sclerosis"
      },
      {
        "code" : "300751",
        "display" : "Familial dilated cardiomyopathy with conduction defect due to LMNA mutation"
      },
      {
        "code" : "3008",
        "display" : "Pyruvate carboxylase deficiency"
      },
      {
        "code" : "300849",
        "display" : "Diffuse large B-cell lymphoma of the central nervous system"
      },
      {
        "code" : "300857",
        "display" : "T-cell/histiocyte rich large B cell lymphoma"
      },
      {
        "code" : "300865",
        "display" : "Primary cutaneous anaplastic large cell lymphoma"
      },
      {
        "code" : "300869",
        "display" : "Splenic diffuse red pulp small B-cell lymphoma"
      },
      {
        "code" : "300878",
        "display" : "Hairy cell leukemia variant"
      },
      {
        "code" : "300888",
        "display" : "Diffuse large B-cell lymphoma with chronic inflammation"
      },
      {
        "code" : "300895",
        "display" : "ALK-positive anaplastic large cell lymphoma"
      },
      {
        "code" : "300903",
        "display" : "ALK-negative anaplastic large cell lymphoma"
      },
      {
        "code" : "3010",
        "display" : "Qazi-Markouizos syndrome"
      },
      {
        "code" : "3011",
        "display" : "Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome"
      },
      {
        "code" : "3015",
        "display" : "Radio-renal syndrome"
      },
      {
        "code" : "3016",
        "display" : "Absent radius-anogenital anomalies syndrome"
      },
      {
        "code" : "3018",
        "display" : "Retinal ischemic syndrome-digestive tract small vessel hyalinosis-diffuse cerebral calcifications syndrome"
      },
      {
        "code" : "3019",
        "display" : "Ramon syndrome"
      },
      {
        "code" : "302",
        "display" : "Inherited epidermodysplasia verruciformis"
      },
      {
        "code" : "3020",
        "display" : "Ramsay Hunt syndrome"
      },
      {
        "code" : "3021",
        "display" : "RAPADILINO syndrome"
      },
      {
        "code" : "3023",
        "display" : "External auditory canal atresia-vertical talus-hypertelorism syndrome"
      },
      {
        "code" : "3026",
        "display" : "Radial ray hypoplasia-choanal atresia syndrome"
      },
      {
        "code" : "3027",
        "display" : "Caudal regression syndrome"
      },
      {
        "code" : "3032",
        "display" : "NPHP3-related Meckel-like syndrome"
      },
      {
        "code" : "3033",
        "display" : "Renal tubular dysgenesis"
      },
      {
        "code" : "3034",
        "display" : "Delayed membranous cranial ossification"
      },
      {
        "code" : "3035",
        "display" : "Growth delay-hydrocephaly-lung hypoplasia syndrome"
      },
      {
        "code" : "3038",
        "display" : "Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome"
      },
      {
        "code" : "30391",
        "display" : "Isolated biliary atresia"
      },
      {
        "code" : "3041",
        "display" : "Intellectual disability-balding-patella luxation-acromicria syndrome"
      },
      {
        "code" : "3042",
        "display" : "Intellectual disability-cataracts-calcified pinnae-myopathy syndrome"
      },
      {
        "code" : "3044",
        "display" : "Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome"
      },
      {
        "code" : "3047",
        "display" : "Blepharophimosis-intellectual disability syndrome, SBBYS type"
      },
      {
        "code" : "3051",
        "display" : "Nicolaides-Baraitser syndrome"
      },
      {
        "code" : "3052",
        "display" : "X-linked intellectual disability-seizures-psoriasis syndrome"
      },
      {
        "code" : "3055",
        "display" : "X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome"
      },
      {
        "code" : "3057",
        "display" : "Monoamine oxidase A deficiency"
      },
      {
        "code" : "306",
        "display" : "Self-limited infantile epilepsy"
      },
      {
        "code" : "3063",
        "display" : "X-linked intellectual disability, Snyder type"
      },
      {
        "code" : "306431",
        "display" : "Adult-onset immunodeficiency with anti-interferon-gamma autoantibodies"
      },
      {
        "code" : "306498",
        "display" : "PTEN hamartoma tumor syndrome"
      },
      {
        "code" : "306504",
        "display" : "Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome"
      },
      {
        "code" : "306511",
        "display" : "Autosomal recessive spastic paraplegia type 48"
      },
      {
        "code" : "306516",
        "display" : "Primary hypomagnesemia with hypercalciuria and nephrocalcinosis"
      },
      {
        "code" : "306527",
        "display" : "Isolated hereditary congenital facial paralysis"
      },
      {
        "code" : "306530",
        "display" : "Congenital hereditary facial paralysis-variable hearing loss syndrome"
      },
      {
        "code" : "306542",
        "display" : "Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome"
      },
      {
        "code" : "306547",
        "display" : "Porencephaly-microcephaly-bilateral congenital cataract syndrome"
      },
      {
        "code" : "306550",
        "display" : "FADD-related immunodeficiency"
      },
      {
        "code" : "306553",
        "display" : "Myospherulosis"
      },
      {
        "code" : "306558",
        "display" : "Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome"
      },
      {
        "code" : "306577",
        "display" : "Hereditary sodium channelopathy-related small fibers neuropathy"
      },
      {
        "code" : "306617",
        "display" : "X-linked complicated spastic paraplegia type 1"
      },
      {
        "code" : "306644",
        "display" : "Complication after organ transplantation"
      },
      {
        "code" : "306658",
        "display" : "Familial normophosphatemic tumoral calcinosis"
      },
      {
        "code" : "306661",
        "display" : "Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome"
      },
      {
        "code" : "306669",
        "display" : "Hemiparkinsonism-hemiatrophy syndrome"
      },
      {
        "code" : "306674",
        "display" : "Kufor-Rakeb syndrome"
      },
      {
        "code" : "306682",
        "display" : "Manganese poisoning"
      },
      {
        "code" : "306686",
        "display" : "Delayed encephalopathy due to carbon monoxide poisoning"
      },
      {
        "code" : "306692",
        "display" : "Cyanide-induced parkinsonism-dystonia"
      },
      {
        "code" : "306731",
        "display" : "Sydenham chorea"
      },
      {
        "code" : "306734",
        "display" : "Primary dystonia, DYT21 type"
      },
      {
        "code" : "306741",
        "display" : "Hemidystonia-hemiatrophy syndrome"
      },
      {
        "code" : "306776",
        "display" : "Sporadic hyperekplexia"
      },
      {
        "code" : "3068",
        "display" : "Intellectual disability-myopathy-short stature-endocrine defect syndrome"
      },
      {
        "code" : "307",
        "display" : "Juvenile myoclonic epilepsy"
      },
      {
        "code" : "3071",
        "display" : "Costello syndrome"
      },
      {
        "code" : "3074",
        "display" : "Intellectual disability-short stature-hypertelorism syndrome"
      },
      {
        "code" : "3077",
        "display" : "X-linked intellectual disability-psychosis-macroorchidism syndrome"
      },
      {
        "code" : "307766",
        "display" : "Curly hair-acral keratoderma-caries syndrome"
      },
      {
        "code" : "3078",
        "display" : "Severe X-linked intellectual disability, Gustavson type"
      },
      {
        "code" : "3079",
        "display" : "Intellectual disability, Buenos-Aires type"
      },
      {
        "code" : "307936",
        "display" : "Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome"
      },
      {
        "code" : "308",
        "display" : "Progressive myoclonic epilepsy type 1"
      },
      {
        "code" : "3080",
        "display" : "Intellectual disability, Wolff type"
      },
      {
        "code" : "308013",
        "display" : "Focal acral hyperkeratosis"
      },
      {
        "code" : "3082",
        "display" : "Intellectual disability-polydactyly-uncombable hair syndrome"
      },
      {
        "code" : "308380",
        "display" : "Methylcobalamin deficiency type cblDv1"
      },
      {
        "code" : "308386",
        "display" : "Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A"
      },
      {
        "code" : "308393",
        "display" : "Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B"
      },
      {
        "code" : "308400",
        "display" : "Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C"
      },
      {
        "code" : "308410",
        "display" : "Autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency"
      },
      {
        "code" : "308425",
        "display" : "Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency"
      },
      {
        "code" : "308442",
        "display" : "Vitamin B12-responsive methylmalonic acidemia, type cblDv2"
      },
      {
        "code" : "308473",
        "display" : "Erythrocyte galactose epimerase deficiency"
      },
      {
        "code" : "308487",
        "display" : "Generalized galactose epimerase deficiency"
      },
      {
        "code" : "3085",
        "display" : "Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome"
      },
      {
        "code" : "308552",
        "display" : "Glycogen storage disease due to acid maltase deficiency, infantile onset"
      },
      {
        "code" : "3086",
        "display" : "Autosomal dominant vitreoretinochoroidopathy"
      },
      {
        "code" : "308621",
        "display" : "Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form"
      },
      {
        "code" : "308638",
        "display" : "Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form"
      },
      {
        "code" : "308655",
        "display" : "Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form"
      },
      {
        "code" : "308670",
        "display" : "Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form"
      },
      {
        "code" : "308684",
        "display" : "Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form"
      },
      {
        "code" : "308698",
        "display" : "Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form"
      },
      {
        "code" : "308712",
        "display" : "Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form"
      },
      {
        "code" : "3088",
        "display" : "Revesz syndrome"
      },
      {
        "code" : "309015",
        "display" : "Familial lipoprotein lipase deficiency"
      },
      {
        "code" : "309020",
        "display" : "Familial apolipoprotein C-II deficiency"
      },
      {
        "code" : "309025",
        "display" : "Mevalonate kinase deficiency"
      },
      {
        "code" : "309031",
        "display" : "Pancreatic triacylglycerol lipase deficiency"
      },
      {
        "code" : "309108",
        "display" : "Pancreatic colipase deficiency"
      },
      {
        "code" : "309111",
        "display" : "Combined pancreatic lipase-colipase deficiency"
      },
      {
        "code" : "309147",
        "display" : "Hyper-beta-alaninemia"
      },
      {
        "code" : "309155",
        "display" : "Sandhoff disease, infantile form"
      },
      {
        "code" : "309162",
        "display" : "Sandhoff disease, juvenile form"
      },
      {
        "code" : "309169",
        "display" : "Sandhoff disease, adult form"
      },
      {
        "code" : "309178",
        "display" : "Tay-Sachs disease, infantile form"
      },
      {
        "code" : "309185",
        "display" : "Tay-Sachs disease, juvenile form"
      },
      {
        "code" : "309192",
        "display" : "Tay-Sachs disease, adult form"
      },
      {
        "code" : "3092",
        "display" : "Fixed subaortic stenosis"
      },
      {
        "code" : "30924",
        "display" : "Primary hypomagnesemia with secondary hypocalcemia"
      },
      {
        "code" : "309246",
        "display" : "GM2 gangliosidosis, AB variant"
      },
      {
        "code" : "30925",
        "display" : "Hereditary arginine vasopressin deficiency"
      },
      {
        "code" : "309252",
        "display" : "Atypical Gaucher disease due to saposin C deficiency"
      },
      {
        "code" : "309256",
        "display" : "Metachromatic leukodystrophy, late infantile form"
      },
      {
        "code" : "309263",
        "display" : "Metachromatic leukodystrophy, juvenile form"
      },
      {
        "code" : "309271",
        "display" : "Metachromatic leukodystrophy, adult form"
      },
      {
        "code" : "309282",
        "display" : "Alpha-mannosidosis, infantile form"
      },
      {
        "code" : "309288",
        "display" : "Alpha-mannosidosis, adult form"
      },
      {
        "code" : "309297",
        "display" : "Mucopolysaccharidosis type 4A"
      },
      {
        "code" : "3093",
        "display" : "Congenital aortic valve stenosis"
      },
      {
        "code" : "309310",
        "display" : "Mucopolysaccharidosis type 4B"
      },
      {
        "code" : "309324",
        "display" : "Free sialic acid storage disease, infantile form"
      },
      {
        "code" : "309331",
        "display" : "Intermediate severe Salla disease"
      },
      {
        "code" : "309334",
        "display" : "Salla disease"
      },
      {
        "code" : "3095",
        "display" : "Atypical Rett syndrome"
      },
      {
        "code" : "3096",
        "display" : "Reye syndrome"
      },
      {
        "code" : "3097",
        "display" : "Meacham syndrome"
      },
      {
        "code" : "309789",
        "display" : "Rhizomelic chondrodysplasia punctata type 1"
      },
      {
        "code" : "309796",
        "display" : "Rhizomelic chondrodysplasia punctata type 2"
      },
      {
        "code" : "3098",
        "display" : "Rhizomelic syndrome, Urbach type"
      },
      {
        "code" : "309803",
        "display" : "Rhizomelic chondrodysplasia punctata type 3"
      },
      {
        "code" : "309854",
        "display" : "Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome"
      },
      {
        "code" : "3099",
        "display" : "Rheumatic fever"
      },
      {
        "code" : "31",
        "display" : "Oxoglutaric aciduria"
      },
      {
        "code" : "3101",
        "display" : "Richieri Costa-da Silva syndrome"
      },
      {
        "code" : "3102",
        "display" : "Richieri Costa-Pereira syndrome"
      },
      {
        "code" : "3103",
        "display" : "Roberts syndrome"
      },
      {
        "code" : "3104",
        "display" : "Robin sequence-oligodactyly syndrome"
      },
      {
        "code" : "31043",
        "display" : "Primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement"
      },
      {
        "code" : "3107",
        "display" : "Autosomal dominant Robinow syndrome"
      },
      {
        "code" : "3109",
        "display" : "Mayer-Rokitansky-Küster-Hauser syndrome"
      },
      {
        "code" : "3110",
        "display" : "Rombo syndrome"
      },
      {
        "code" : "3111",
        "display" : "Rotor syndrome"
      },
      {
        "code" : "31112",
        "display" : "Dermatofibrosarcoma protuberans"
      },
      {
        "code" : "3115",
        "display" : "Roussy-Lévy syndrome"
      },
      {
        "code" : "31150",
        "display" : "Tangier disease"
      },
      {
        "code" : "312",
        "display" : "Autosomal dominant epidermolytic ichthyosis"
      },
      {
        "code" : "31202",
        "display" : "Melioidosis"
      },
      {
        "code" : "31204",
        "display" : "Nocardiosis"
      },
      {
        "code" : "31205",
        "display" : "Rat-bite fever"
      },
      {
        "code" : "3121",
        "display" : "Ruvalcaba syndrome"
      },
      {
        "code" : "3124",
        "display" : "Saccharopinuria"
      },
      {
        "code" : "3129",
        "display" : "Sarcosinemia"
      },
      {
        "code" : "313",
        "display" : "Lamellar ichthyosis"
      },
      {
        "code" : "3130",
        "display" : "Satoyoshi syndrome"
      },
      {
        "code" : "3132",
        "display" : "Say-Barber-Miller syndrome"
      },
      {
        "code" : "3134",
        "display" : "SCARF syndrome"
      },
      {
        "code" : "3137",
        "display" : "Alpha-N-acetylgalactosaminidase deficiency"
      },
      {
        "code" : "313772",
        "display" : "Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome"
      },
      {
        "code" : "313781",
        "display" : "20p13 microdeletion syndrome"
      },
      {
        "code" : "313795",
        "display" : "Jawad syndrome"
      },
      {
        "code" : "3138",
        "display" : "Ulnar-mammary syndrome"
      },
      {
        "code" : "313800",
        "display" : "Retinal dystrophy-optic nerve edema-splenomegaly-anhidrosis-migraine headache syndrome"
      },
      {
        "code" : "313808",
        "display" : "Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia"
      },
      {
        "code" : "313838",
        "display" : "Coats plus syndrome"
      },
      {
        "code" : "313846",
        "display" : "Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome"
      },
      {
        "code" : "313850",
        "display" : "Infantile cerebellar-retinal degeneration"
      },
      {
        "code" : "313855",
        "display" : "FGFR2-related bent bone dysplasia"
      },
      {
        "code" : "313884",
        "display" : "12p12.1 microdeletion syndrome"
      },
      {
        "code" : "313892",
        "display" : "Developmental and speech delay due to SOX5 deficiency"
      },
      {
        "code" : "313906",
        "display" : "Congenital pancreatic cyst"
      },
      {
        "code" : "313920",
        "display" : "Epstein-Barr virus-associated gastric carcinoma"
      },
      {
        "code" : "313936",
        "display" : "PENS syndrome"
      },
      {
        "code" : "313947",
        "display" : "2q23.1 microduplication syndrome"
      },
      {
        "code" : "314",
        "display" : "Erythroderma desquamativum"
      },
      {
        "code" : "314002",
        "display" : "Contractures-webbed neck-micrognathia-hypoplastic nipples syndrome"
      },
      {
        "code" : "314017",
        "display" : "Idiopathic linear interstitial keratitis"
      },
      {
        "code" : "314022",
        "display" : "Gastric adenocarcinoma and proximal polyposis of the stomach"
      },
      {
        "code" : "314029",
        "display" : "High bone mass osteogenesis imperfecta"
      },
      {
        "code" : "314034",
        "display" : "7p22.1 microduplication syndrome"
      },
      {
        "code" : "314041",
        "display" : "Marfanoid habitus-inguinal hernia-advanced bone age syndrome"
      },
      {
        "code" : "314051",
        "display" : "Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome"
      },
      {
        "code" : "3143",
        "display" : "Autoimmune polyendocrinopathy type 2"
      },
      {
        "code" : "314373",
        "display" : "Chronic infantile diarrhea due to guanylate cyclase 2C overactivity"
      },
      {
        "code" : "314376",
        "display" : "Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency"
      },
      {
        "code" : "314381",
        "display" : "Hereditary sensory and autonomic neuropathy type 6"
      },
      {
        "code" : "314389",
        "display" : "Xq12-q13.3 duplication syndrome"
      },
      {
        "code" : "314394",
        "display" : "Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome"
      },
      {
        "code" : "314399",
        "display" : "Autosomal dominant aplasia and myelodysplasia"
      },
      {
        "code" : "3144",
        "display" : "Schneckenbecken dysplasia"
      },
      {
        "code" : "314404",
        "display" : "Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome"
      },
      {
        "code" : "314419",
        "display" : "Ameloblastoma"
      },
      {
        "code" : "314422",
        "display" : "Ameloblastic carcinoma"
      },
      {
        "code" : "314432",
        "display" : "Spigelian hernia-cryptorchidism syndrome"
      },
      {
        "code" : "314451",
        "display" : "Meigs syndrome"
      },
      {
        "code" : "314459",
        "display" : "Pseudo-Meigs syndrome"
      },
      {
        "code" : "314466",
        "display" : "Atypical Meigs syndrome"
      },
      {
        "code" : "314473",
        "display" : "Ovarian fibroma"
      },
      {
        "code" : "314478",
        "display" : "Ovarian fibrothecoma"
      },
      {
        "code" : "314485",
        "display" : "Young adult-onset distal hereditary motor neuropathy"
      },
      {
        "code" : "3145",
        "display" : "Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome"
      },
      {
        "code" : "314555",
        "display" : "Facial dysmorphism-ocular anomalies-osteopenia-intellectual disability-dental anomalies syndrome"
      },
      {
        "code" : "314566",
        "display" : "Primary progressive apraxia of speech"
      },
      {
        "code" : "314572",
        "display" : "Autosomal recessive leukoencephalopathy-ischemic stroke-retinitis pigmentosa syndrome"
      },
      {
        "code" : "314575",
        "display" : "Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome"
      },
      {
        "code" : "314585",
        "display" : "15q overgrowth syndrome"
      },
      {
        "code" : "314588",
        "display" : "Distal triplication 15q syndrome"
      },
      {
        "code" : "314597",
        "display" : "Chudley-McCullough syndrome"
      },
      {
        "code" : "314603",
        "display" : "Autosomal recessive spastic ataxia with leukoencephalopathy"
      },
      {
        "code" : "314613",
        "display" : "Growing teratoma syndrome"
      },
      {
        "code" : "314621",
        "display" : "Duplication of the pituitary gland"
      },
      {
        "code" : "314629",
        "display" : "CLN11 disease"
      },
      {
        "code" : "314632",
        "display" : "CLN12 disease"
      },
      {
        "code" : "314637",
        "display" : "Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency"
      },
      {
        "code" : "314647",
        "display" : "Non-progressive cerebellar ataxia with intellectual disability"
      },
      {
        "code" : "314652",
        "display" : "Variant ABeta2M amyloidosis"
      },
      {
        "code" : "314655",
        "display" : "Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion"
      },
      {
        "code" : "314662",
        "display" : "Segmental progressive overgrowth syndrome with fibroadipose hyperplasia"
      },
      {
        "code" : "314667",
        "display" : "TMEM165-CDG"
      },
      {
        "code" : "314679",
        "display" : "Cerebrofacioarticular syndrome"
      },
      {
        "code" : "314684",
        "display" : "Primary bone lymphoma"
      },
      {
        "code" : "314689",
        "display" : "Combined immunodeficiency due to STK4 deficiency"
      },
      {
        "code" : "314697",
        "display" : "Acquired porencephaly"
      },
      {
        "code" : "314701",
        "display" : "Primary systemic amyloidosis"
      },
      {
        "code" : "314709",
        "display" : "Primary localized amyloidosis"
      },
      {
        "code" : "314718",
        "display" : "Lethal arteriopathy syndrome due to fibulin-4 deficiency"
      },
      {
        "code" : "314721",
        "display" : "Atypical dentin dysplasia due to SMOC2 deficiency"
      },
      {
        "code" : "314769",
        "display" : "Somatomammotropinoma"
      },
      {
        "code" : "314777",
        "display" : "Familial isolated pituitary adenoma"
      },
      {
        "code" : "314786",
        "display" : "Silent pituitary adenoma"
      },
      {
        "code" : "314790",
        "display" : "Null pituitary adenoma"
      },
      {
        "code" : "314795",
        "display" : "SHOX-related short stature"
      },
      {
        "code" : "3148",
        "display" : "Malignant peripheral nerve sheath tumor"
      },
      {
        "code" : "314802",
        "display" : "Short stature due to partial GHR deficiency"
      },
      {
        "code" : "314811",
        "display" : "Short stature due to GHSR deficiency"
      },
      {
        "code" : "314889",
        "display" : "Autosomal dominant proximal renal tubular acidosis"
      },
      {
        "code" : "314911",
        "display" : "Severe Canavan disease"
      },
      {
        "code" : "314918",
        "display" : "Mild Canavan disease"
      },
      {
        "code" : "314950",
        "display" : "Primary hypereosinophilic syndrome"
      },
      {
        "code" : "314962",
        "display" : "Secondary hypereosinophilic syndrome"
      },
      {
        "code" : "314970",
        "display" : "Lymphocytic hypereosinophilic syndrome"
      },
      {
        "code" : "314978",
        "display" : "X-linked non progressive cerebellar ataxia"
      },
      {
        "code" : "314993",
        "display" : "Cataract-congenital heart disease-neural tube defect syndrome"
      },
      {
        "code" : "315",
        "display" : "Erythrokeratoderma ''en cocardes''"
      },
      {
        "code" : "3151",
        "display" : "Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome"
      },
      {
        "code" : "3152",
        "display" : "Sclerosteosis"
      },
      {
        "code" : "315306",
        "display" : "Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form"
      },
      {
        "code" : "315311",
        "display" : "Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form"
      },
      {
        "code" : "3156",
        "display" : "Senior-Loken syndrome"
      },
      {
        "code" : "3157",
        "display" : "Septo-optic dysplasia spectrum"
      },
      {
        "code" : "316",
        "display" : "Progressive symmetric erythrokeratodermia"
      },
      {
        "code" : "3161",
        "display" : "Congenital pulmonary sequestration"
      },
      {
        "code" : "3162",
        "display" : "Sézary syndrome"
      },
      {
        "code" : "3163",
        "display" : "SHORT syndrome"
      },
      {
        "code" : "3164",
        "display" : "Omphalocele syndrome, Shprintzen-Goldberg type"
      },
      {
        "code" : "3165",
        "display" : "Eosinophilic fasciitis"
      },
      {
        "code" : "3166",
        "display" : "Sialuria"
      },
      {
        "code" : "3167",
        "display" : "Siegler-Brewer-Carey syndrome"
      },
      {
        "code" : "3168",
        "display" : "Sillence syndrome"
      },
      {
        "code" : "3169",
        "display" : "Sirenomelia"
      },
      {
        "code" : "317",
        "display" : "Erythrokeratodermia variabilis"
      },
      {
        "code" : "31709",
        "display" : "Infantile convulsions and choreoathetosis"
      },
      {
        "code" : "3172",
        "display" : "Eyebrow duplication-syndactyly syndrome"
      },
      {
        "code" : "3173",
        "display" : "Infantile spasms-broad thumbs syndrome"
      },
      {
        "code" : "31740",
        "display" : "Hypersensitivity pneumonitis"
      },
      {
        "code" : "317425",
        "display" : "Severe combined immunodeficiency due to DNA-PKcs deficiency"
      },
      {
        "code" : "317428",
        "display" : "Combined immunodeficiency due to ORAI1 deficiency"
      },
      {
        "code" : "317430",
        "display" : "Combined immunodeficiency due to STIM1 deficiency"
      },
      {
        "code" : "317473",
        "display" : "Common variable immunodeficiency phenotype due to IKAROS functional haploinsufficiency"
      },
      {
        "code" : "317476",
        "display" : "XMEN"
      },
      {
        "code" : "3175",
        "display" : "X-linked spasticity-intellectual disability-epilepsy syndrome"
      },
      {
        "code" : "3176",
        "display" : "Spina bifida-hypospadias syndrome"
      },
      {
        "code" : "3177",
        "display" : "Spinocerebellar degeneration-corneal dystrophy syndrome"
      },
      {
        "code" : "318",
        "display" : "Acute erythroid leukemia"
      },
      {
        "code" : "3180",
        "display" : "Spondylocamptodactyly syndrome"
      },
      {
        "code" : "3181",
        "display" : "Sprengel deformity"
      },
      {
        "code" : "31824",
        "display" : "Colchicine poisoning"
      },
      {
        "code" : "31825",
        "display" : "Methanol poisoning"
      },
      {
        "code" : "31826",
        "display" : "Ethylene glycol poisoning"
      },
      {
        "code" : "31827",
        "display" : "Paraquat poisoning"
      },
      {
        "code" : "31828",
        "display" : "Digitalis poisoning"
      },
      {
        "code" : "31837",
        "display" : "Pulmonary venoocclusive disease"
      },
      {
        "code" : "3184",
        "display" : "Steatocystoma multiplex-natal teeth syndrome"
      },
      {
        "code" : "3186",
        "display" : "Holoprosencephaly-radial heart renal anomalies syndrome"
      },
      {
        "code" : "3189",
        "display" : "Congenital pulmonary valvar stenosis"
      },
      {
        "code" : "319",
        "display" : "Skeletal Ewing sarcoma"
      },
      {
        "code" : "3190",
        "display" : "Subpulmonary stenosis"
      },
      {
        "code" : "3191",
        "display" : "Subaortic stenosis-short stature syndrome"
      },
      {
        "code" : "319160",
        "display" : "Congenital myopathy with internal nuclei and atypical cores"
      },
      {
        "code" : "319171",
        "display" : "Distal 17p13.1 microdeletion syndrome"
      },
      {
        "code" : "319182",
        "display" : "Wiedemann-Steiner syndrome"
      },
      {
        "code" : "319189",
        "display" : "Familial cortical myoclonus"
      },
      {
        "code" : "319192",
        "display" : "Diencephalic-mesencephalic junction dysplasia"
      },
      {
        "code" : "319195",
        "display" : "Chondroectodermal dysplasia with night blindness"
      },
      {
        "code" : "319199",
        "display" : "Autosomal recessive spastic paraplegia type 53"
      },
      {
        "code" : "3192",
        "display" : "Supravalvular pulmonary stenosis"
      },
      {
        "code" : "319205",
        "display" : "Bilateral massive adrenal hemorrhage"
      },
      {
        "code" : "319213",
        "display" : "Lujo hemorrhagic fever"
      },
      {
        "code" : "319218",
        "display" : "Ebola hemorrhagic fever"
      },
      {
        "code" : "319223",
        "display" : "Argentine hemorrhagic fever"
      },
      {
        "code" : "319229",
        "display" : "Bolivian hemorrhagic fever"
      },
      {
        "code" : "319234",
        "display" : "Venezuelan hemorrhagic fever"
      },
      {
        "code" : "319239",
        "display" : "Brazilian hemorrhagic fever"
      },
      {
        "code" : "319244",
        "display" : "Chapare hemorrhagic fever"
      },
      {
        "code" : "319247",
        "display" : "Hantavirus pulmonary syndrome"
      },
      {
        "code" : "319251",
        "display" : "Rift valley fever"
      },
      {
        "code" : "319254",
        "display" : "Kyasanur forest disease"
      },
      {
        "code" : "319266",
        "display" : "Omsk hemorrhagic fever"
      },
      {
        "code" : "319276",
        "display" : "Clear cell renal carcinoma"
      },
      {
        "code" : "319287",
        "display" : "Multilocular cystic renal neoplasm of low malignant potential"
      },
      {
        "code" : "319298",
        "display" : "Papillary renal cell carcinoma"
      },
      {
        "code" : "3193",
        "display" : "Supravalvular aortic stenosis"
      },
      {
        "code" : "319303",
        "display" : "Chromophobe renal cell carcinoma"
      },
      {
        "code" : "319308",
        "display" : "MiT family translocation renal cell carcinoma"
      },
      {
        "code" : "319319",
        "display" : "Renal medullary carcinoma"
      },
      {
        "code" : "319322",
        "display" : "Mucinous tubular and spindle cell renal carcinoma"
      },
      {
        "code" : "319325",
        "display" : "Tubulocystic renal cell carcinoma"
      },
      {
        "code" : "319332",
        "display" : "Autosomal recessive myogenic arthrogryposis multiplex congenita"
      },
      {
        "code" : "319340",
        "display" : "Carney complex-trismus-pseudocamptodactyly syndrome"
      },
      {
        "code" : "3194",
        "display" : "Corneodermatoosseous syndrome"
      },
      {
        "code" : "319462",
        "display" : "Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations"
      },
      {
        "code" : "319465",
        "display" : "Inherited acute myeloid leukemia"
      },
      {
        "code" : "319480",
        "display" : "Acute myeloid leukemia with CEBPA somatic mutations"
      },
      {
        "code" : "319487",
        "display" : "Familial papillary or follicular thyroid carcinoma"
      },
      {
        "code" : "319504",
        "display" : "Combined oxidative phosphorylation defect type 8"
      },
      {
        "code" : "319509",
        "display" : "Combined oxidative phosphorylation defect type 9"
      },
      {
        "code" : "319514",
        "display" : "Combined oxidative phosphorylation defect type 13"
      },
      {
        "code" : "319519",
        "display" : "Combined oxidative phosphorylation defect type 14"
      },
      {
        "code" : "319524",
        "display" : "Combined oxidative phosphorylation defect type 15"
      },
      {
        "code" : "319547",
        "display" : "Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency"
      },
      {
        "code" : "319552",
        "display" : "Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency"
      },
      {
        "code" : "319558",
        "display" : "Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency"
      },
      {
        "code" : "319563",
        "display" : "Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency"
      },
      {
        "code" : "319569",
        "display" : "Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency"
      },
      {
        "code" : "319574",
        "display" : "Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency"
      },
      {
        "code" : "319581",
        "display" : "Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency"
      },
      {
        "code" : "319589",
        "display" : "Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency"
      },
      {
        "code" : "319595",
        "display" : "Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency"
      },
      {
        "code" : "3196",
        "display" : "Steroid dehydrogenase deficiency-dental anomalies syndrome"
      },
      {
        "code" : "319600",
        "display" : "Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency"
      },
      {
        "code" : "319605",
        "display" : "X-linked mendelian susceptibility to mycobacterial diseases"
      },
      {
        "code" : "319635",
        "display" : "Amyloidosis cutis dyschromia"
      },
      {
        "code" : "319640",
        "display" : "Retinal macular dystrophy type 2"
      },
      {
        "code" : "319646",
        "display" : "PGM1-CDG"
      },
      {
        "code" : "319651",
        "display" : "Constitutional megaloblastic anemia with severe neurologic disease"
      },
      {
        "code" : "319667",
        "display" : "Primary lymphoma of the conjunctiva"
      },
      {
        "code" : "319671",
        "display" : "Alazami syndrome"
      },
      {
        "code" : "319675",
        "display" : "Microcephalic primordial dwarfism, Dauber type"
      },
      {
        "code" : "319678",
        "display" : "Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome"
      },
      {
        "code" : "3197",
        "display" : "Hereditary hyperekplexia"
      },
      {
        "code" : "3198",
        "display" : "Stiff person spectrum disorder"
      },
      {
        "code" : "3199",
        "display" : "Stimmler syndrome"
      },
      {
        "code" : "32",
        "display" : "Glutathione synthetase deficiency"
      },
      {
        "code" : "320",
        "display" : "Apparent mineralocorticoid excess"
      },
      {
        "code" : "3200",
        "display" : "Arthrogryposis-ectodermal dysplasia syndrome"
      },
      {
        "code" : "3201",
        "display" : "Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome"
      },
      {
        "code" : "3202",
        "display" : "Dehydrated hereditary stomatocytosis"
      },
      {
        "code" : "3203",
        "display" : "Overhydrated hereditary stomatocytosis"
      },
      {
        "code" : "320355",
        "display" : "Autosomal dominant spastic paraplegia type 41"
      },
      {
        "code" : "320360",
        "display" : "MT-ATP6-related mitochondrial spastic paraplegia"
      },
      {
        "code" : "320365",
        "display" : "Autosomal dominant spastic paraplegia type 36"
      },
      {
        "code" : "320370",
        "display" : "Autosomal recessive spastic paraplegia type 43"
      },
      {
        "code" : "320375",
        "display" : "Autosomal recessive spastic paraplegia type 55"
      },
      {
        "code" : "320380",
        "display" : "Autosomal recessive spastic paraplegia type 54"
      },
      {
        "code" : "320385",
        "display" : "Hereditary sensory and autonomic neuropathy due to TECPR2 mutation"
      },
      {
        "code" : "320391",
        "display" : "Autosomal recessive spastic paraplegia type 46"
      },
      {
        "code" : "320396",
        "display" : "Autosomal recessive spastic paraplegia type 45"
      },
      {
        "code" : "3204",
        "display" : "Stormorken-Sjaastad-Langslet syndrome"
      },
      {
        "code" : "320401",
        "display" : "Autosomal recessive spastic paraplegia type 44"
      },
      {
        "code" : "320406",
        "display" : "Spastic paraplegia-optic atrophy-neuropathy syndrome"
      },
      {
        "code" : "320411",
        "display" : "Autosomal recessive spastic paraplegia type 56"
      },
      {
        "code" : "3205",
        "display" : "Sturge-Weber syndrome"
      },
      {
        "code" : "3206",
        "display" : "Stüve-Wiedemann syndrome"
      },
      {
        "code" : "3207",
        "display" : "White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome"
      },
      {
        "code" : "3208",
        "display" : "Isolated succinate-CoQ reductase deficiency"
      },
      {
        "code" : "321",
        "display" : "Multiple osteochondromas"
      },
      {
        "code" : "3214",
        "display" : "Deaf blind hypopigmentation syndrome, Yemenite type"
      },
      {
        "code" : "3216",
        "display" : "Conductive deafness-malformed external ear syndrome"
      },
      {
        "code" : "3217",
        "display" : "Deafness-small bowel diverticulosis-neuropathy syndrome"
      },
      {
        "code" : "3218",
        "display" : "Deafness-epiphyseal dysplasia-short stature syndrome"
      },
      {
        "code" : "3219",
        "display" : "Fountain syndrome"
      },
      {
        "code" : "322",
        "display" : "Exstrophy-epispadias complex"
      },
      {
        "code" : "3220",
        "display" : "Deafness-enamel hypoplasia-nail defects syndrome"
      },
      {
        "code" : "3222",
        "display" : "Phosphoribosylpyrophosphate synthetase superactivity"
      },
      {
        "code" : "3224",
        "display" : "Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome"
      },
      {
        "code" : "3225",
        "display" : "Hearing loss-familial salivary gland insensitivity to aldosterone syndrome"
      },
      {
        "code" : "3230",
        "display" : "Deafness-oligodontia syndrome"
      },
      {
        "code" : "3232",
        "display" : "Deafness-ear malformation-facial palsy syndrome"
      },
      {
        "code" : "3233",
        "display" : "Cochleosaccular degeneration-cataract syndrome"
      },
      {
        "code" : "3235",
        "display" : "Progressive deafness with stapes fixation"
      },
      {
        "code" : "3236",
        "display" : "Conductive deafness-ptosis-skeletal anomalies syndrome"
      },
      {
        "code" : "3237",
        "display" : "Multiple synostoses syndrome"
      },
      {
        "code" : "3238",
        "display" : "Cardiospondylocarpofacial syndrome"
      },
      {
        "code" : "3239",
        "display" : "Deafness-vitiligo-achalasia syndrome"
      },
      {
        "code" : "324",
        "display" : "Fabry disease"
      },
      {
        "code" : "3240",
        "display" : "Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome"
      },
      {
        "code" : "3241",
        "display" : "Deafness-craniofacial syndrome"
      },
      {
        "code" : "3242",
        "display" : "Renpenning syndrome"
      },
      {
        "code" : "324262",
        "display" : "Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency"
      },
      {
        "code" : "324290",
        "display" : "PRDM8-related progressive myoclonus epilepsy"
      },
      {
        "code" : "324294",
        "display" : "T-cell immunodeficiency with epidermodysplasia verruciformis"
      },
      {
        "code" : "324299",
        "display" : "Multiple paragangliomas associated with polycythemia"
      },
      {
        "code" : "3243",
        "display" : "Sweet syndrome"
      },
      {
        "code" : "324307",
        "display" : "Severe lateral tibial bowing-short stature-mild winged scapula-mild facial dysmorphism syndrome"
      },
      {
        "code" : "324313",
        "display" : "9p13 microdeletion syndrome"
      },
      {
        "code" : "324321",
        "display" : "Sinoatrial node dysfunction and deafness"
      },
      {
        "code" : "324353",
        "display" : "Congenital achiasma"
      },
      {
        "code" : "324364",
        "display" : "Mixed sclerosing bone dystrophy with extra-skeletal manifestations"
      },
      {
        "code" : "324381",
        "display" : "Hereditary inclusion body myopathy type 4"
      },
      {
        "code" : "324410",
        "display" : "X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome"
      },
      {
        "code" : "324416",
        "display" : "Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome"
      },
      {
        "code" : "324422",
        "display" : "ALG13-CDG"
      },
      {
        "code" : "324442",
        "display" : "Autosomal recessive axonal neuropathy with neuromyotonia"
      },
      {
        "code" : "324525",
        "display" : "Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation"
      },
      {
        "code" : "324530",
        "display" : "Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation"
      },
      {
        "code" : "324535",
        "display" : "Combined oxidative phosphorylation defect type 11"
      },
      {
        "code" : "324540",
        "display" : "Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome"
      },
      {
        "code" : "324561",
        "display" : "Hypopigmentation-punctate palmoplantar keratoderma syndrome"
      },
      {
        "code" : "324569",
        "display" : "Pontocerebellar hypoplasia type 8"
      },
      {
        "code" : "324575",
        "display" : "Hyperinsulinism due to HNF1A deficiency"
      },
      {
        "code" : "324581",
        "display" : "Benign Samaritan congenital myopathy"
      },
      {
        "code" : "324585",
        "display" : "Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain"
      },
      {
        "code" : "324588",
        "display" : "Familial dyskinesia and facial myokymia"
      },
      {
        "code" : "3246",
        "display" : "Symphalangism with multiple anomalies of hands and feet"
      },
      {
        "code" : "324601",
        "display" : "X-linked cleft palate and ankyloglossia"
      },
      {
        "code" : "324604",
        "display" : "Classic multiminicore myopathy"
      },
      {
        "code" : "324611",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation"
      },
      {
        "code" : "324625",
        "display" : "Chikungunya"
      },
      {
        "code" : "324632",
        "display" : "Hendra virus infection"
      },
      {
        "code" : "324636",
        "display" : "Autoerythrocyte sensitization syndrome"
      },
      {
        "code" : "324648",
        "display" : "Invasive non-typhoidal salmonellosis"
      },
      {
        "code" : "324703",
        "display" : "ABetaL34V amyloidosis"
      },
      {
        "code" : "324708",
        "display" : "ABeta amyloidosis, Iowa type"
      },
      {
        "code" : "324713",
        "display" : "ABeta amyloidosis, Italian type"
      },
      {
        "code" : "324718",
        "display" : "ABetaA21G amyloidosis"
      },
      {
        "code" : "324723",
        "display" : "ABeta amyloidosis, Arctic type"
      },
      {
        "code" : "324737",
        "display" : "SRD5A3-CDG"
      },
      {
        "code" : "3248",
        "display" : "Isolated distal symphalangism"
      },
      {
        "code" : "324964",
        "display" : "Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis"
      },
      {
        "code" : "324972",
        "display" : "MAGIC syndrome"
      },
      {
        "code" : "324977",
        "display" : "Proteasome-associated autoinflammatory syndrome"
      },
      {
        "code" : "325",
        "display" : "Congenital factor II deficiency"
      },
      {
        "code" : "3250",
        "display" : "Proximal symphalangism"
      },
      {
        "code" : "325124",
        "display" : "Testicular agenesis"
      },
      {
        "code" : "3253",
        "display" : "Cleft lip/palate-ectodermal dysplasia syndrome"
      },
      {
        "code" : "325345",
        "display" : "46,XY ovotesticular difference of sex development"
      },
      {
        "code" : "325448",
        "display" : "Leydig cell hypoplasia due to LHB deficiency"
      },
      {
        "code" : "3255",
        "display" : "Filippi syndrome"
      },
      {
        "code" : "325524",
        "display" : "Classic congenital lipoid adrenal hyperplasia due to STAR deficency"
      },
      {
        "code" : "325529",
        "display" : "Non-classic congenital lipoid adrenal hyperplasia due to STAR deficency"
      },
      {
        "code" : "3258",
        "display" : "Cenani-Lenz syndrome"
      },
      {
        "code" : "3259",
        "display" : "Syndactyly-polydactyly-ear lobe syndrome"
      },
      {
        "code" : "326",
        "display" : "Congenital factor V deficiency"
      },
      {
        "code" : "3260",
        "display" : "Idiopathic hypereosinophilic syndrome"
      },
      {
        "code" : "3261",
        "display" : "Autoimmune lymphoproliferative syndrome"
      },
      {
        "code" : "3262",
        "display" : "Dobrow syndrome"
      },
      {
        "code" : "3263",
        "display" : "Syngnathia-cleft palate syndrome"
      },
      {
        "code" : "3265",
        "display" : "Isolated humero-radial synostosis"
      },
      {
        "code" : "3266",
        "display" : "Isolated humero-radio-ulnar synostosis"
      },
      {
        "code" : "3268",
        "display" : "Radioulnar synostosis-microcephaly-scoliosis syndrome"
      },
      {
        "code" : "3269",
        "display" : "Isolated radio-ulnar synostosis"
      },
      {
        "code" : "327",
        "display" : "Congenital factor VII deficiency"
      },
      {
        "code" : "3270",
        "display" : "Radioulnar synostosis-developmental delay-hypotonia syndrome"
      },
      {
        "code" : "3273",
        "display" : "Synovial sarcoma"
      },
      {
        "code" : "3275",
        "display" : "Spondylocarpotarsal synostosis"
      },
      {
        "code" : "328",
        "display" : "Congenital factor X deficiency"
      },
      {
        "code" : "3282",
        "display" : "Multifocal atrial tachycardia"
      },
      {
        "code" : "3283",
        "display" : "His bundle tachycardia"
      },
      {
        "code" : "3286",
        "display" : "Catecholaminergic polymorphic ventricular tachycardia"
      },
      {
        "code" : "3287",
        "display" : "Takayasu arteritis"
      },
      {
        "code" : "329",
        "display" : "Congenital factor XI deficiency"
      },
      {
        "code" : "3291",
        "display" : "Teebi-Shaltout syndrome"
      },
      {
        "code" : "329173",
        "display" : "Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis"
      },
      {
        "code" : "329178",
        "display" : "Congenital muscular dystrophy with intellectual disability and severe epilepsy"
      },
      {
        "code" : "329191",
        "display" : "Tall stature-long halluces-multiple extra-epiphyses syndrome"
      },
      {
        "code" : "329195",
        "display" : "Developmental delay with autism spectrum disorder and gait instability"
      },
      {
        "code" : "3292",
        "display" : "Tel Hashomer camptodactyly syndrome"
      },
      {
        "code" : "329211",
        "display" : "Autosomal dominant neovascular inflammatory vitreoretinopathy"
      },
      {
        "code" : "329217",
        "display" : "Cerebral sinovenous thrombosis"
      },
      {
        "code" : "329224",
        "display" : "Schuurs-Hoeijmakers syndrome"
      },
      {
        "code" : "329228",
        "display" : "Microcephalic primordial dwarfism due to ZNF335 deficiency"
      },
      {
        "code" : "329235",
        "display" : "X-linked central congenital hypothyroidism with late-onset testicular enlargement"
      },
      {
        "code" : "329242",
        "display" : "Congenital chronic diarrhea with protein-losing enteropathy"
      },
      {
        "code" : "329249",
        "display" : "Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency"
      },
      {
        "code" : "329258",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2Q"
      },
      {
        "code" : "329284",
        "display" : "Beta-propeller protein-associated neurodegeneration"
      },
      {
        "code" : "3293",
        "display" : "Telecanthus-hypertelorism-strabismus-pes cavus syndrome"
      },
      {
        "code" : "329308",
        "display" : "Fatty acid hydroxylase-associated neurodegeneration"
      },
      {
        "code" : "329314",
        "display" : "Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency"
      },
      {
        "code" : "329319",
        "display" : "Thrombocythemia with distal limb defects"
      },
      {
        "code" : "329329",
        "display" : "Autosomal recessive frontotemporal pachygyria"
      },
      {
        "code" : "329332",
        "display" : "Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome"
      },
      {
        "code" : "329336",
        "display" : "Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy"
      },
      {
        "code" : "3294",
        "display" : "Extensor tendons of finger anomalies"
      },
      {
        "code" : "329457",
        "display" : "Distal arthrogryposis type 5D"
      },
      {
        "code" : "329466",
        "display" : "Autosomal dominant focal dystonia, DYT25 type"
      },
      {
        "code" : "329469",
        "display" : "Acute megakaryoblastic leukemia in children without Down syndrome"
      },
      {
        "code" : "329475",
        "display" : "Spastic paraplegia-Paget disease of bone syndrome"
      },
      {
        "code" : "329478",
        "display" : "Adult-onset distal myopathy due to VCP mutation"
      },
      {
        "code" : "329481",
        "display" : "Lipoprotein glomerulopathy"
      },
      {
        "code" : "32960",
        "display" : "Tumor necrosis factor receptor 1 associated periodic syndrome"
      },
      {
        "code" : "329802",
        "display" : "5p13 microduplication syndrome"
      },
      {
        "code" : "329813",
        "display" : "Mosaic genome-wide paternal uniparental disomy syndrome"
      },
      {
        "code" : "329874",
        "display" : "Idiopathic giant cell myocarditis"
      },
      {
        "code" : "329883",
        "display" : "Non-hypoproteinemic hypertrophic gastropathy"
      },
      {
        "code" : "329894",
        "display" : "Juvenile overlap myositis"
      },
      {
        "code" : "3299",
        "display" : "Tetanus"
      },
      {
        "code" : "329903",
        "display" : "Immunoglobulin-mediated membranoproliferative glomerulonephritis"
      },
      {
        "code" : "329918",
        "display" : "C3 glomerulopathy"
      },
      {
        "code" : "329931",
        "display" : "C3 glomerulonephritis"
      },
      {
        "code" : "329942",
        "display" : "Transient neonatal multiple acyl-CoA dehydrogenase deficiency"
      },
      {
        "code" : "329967",
        "display" : "Intermittent hydrarthrosis"
      },
      {
        "code" : "329971",
        "display" : "Generalized juvenile polyposis/juvenile polyposis coli"
      },
      {
        "code" : "329977",
        "display" : "Classic neuroendocrine tumor of appendix"
      },
      {
        "code" : "329984",
        "display" : "Goblet cell carcinoma"
      },
      {
        "code" : "33",
        "display" : "Isovaleric acidemia"
      },
      {
        "code" : "330",
        "display" : "Congenital factor XII deficiency"
      },
      {
        "code" : "330001",
        "display" : "Wild type ATTR amyloidosis"
      },
      {
        "code" : "33001",
        "display" : "Lymphedema-distichiasis syndrome"
      },
      {
        "code" : "330012",
        "display" : "High altitude pulmonary edema"
      },
      {
        "code" : "330015",
        "display" : "Lead poisoning"
      },
      {
        "code" : "330021",
        "display" : "Mercury poisoning"
      },
      {
        "code" : "330029",
        "display" : "Hypotrichosis-deafness syndrome"
      },
      {
        "code" : "330032",
        "display" : "Hemoglobin Lepore-beta-thalassemia syndrome"
      },
      {
        "code" : "330041",
        "display" : "Hemoglobin M disease"
      },
      {
        "code" : "330050",
        "display" : "DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect"
      },
      {
        "code" : "330054",
        "display" : "Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome"
      },
      {
        "code" : "330058",
        "display" : "Hydroa vacciniforme"
      },
      {
        "code" : "330061",
        "display" : "Actinic prurigo"
      },
      {
        "code" : "330064",
        "display" : "Chronic actinic dermatitis"
      },
      {
        "code" : "3301",
        "display" : "Tetraamelia-multiple malformations syndrome"
      },
      {
        "code" : "3303",
        "display" : "Tetralogy of Fallot"
      },
      {
        "code" : "3304",
        "display" : "Fallot complex-intellectual disability-growth delay syndrome"
      },
      {
        "code" : "3305",
        "display" : "Tetraploidy syndrome"
      },
      {
        "code" : "3306",
        "display" : "Inverted duplicated chromosome 15 syndrome"
      },
      {
        "code" : "33067",
        "display" : "Metaphyseal chondrodysplasia, Jansen type"
      },
      {
        "code" : "33069",
        "display" : "Dravet syndrome"
      },
      {
        "code" : "3307",
        "display" : "Tetrasomy 18p syndrome"
      },
      {
        "code" : "3309",
        "display" : "Tetrasomy 5p syndrome"
      },
      {
        "code" : "331",
        "display" : "Congenital factor XIII deficiency"
      },
      {
        "code" : "3310",
        "display" : "Tetrasomy 9p syndrome"
      },
      {
        "code" : "33108",
        "display" : "Lethal multiple pterygium syndrome"
      },
      {
        "code" : "33110",
        "display" : "Autosomal non-syndromic agammaglobulinemia"
      },
      {
        "code" : "33111",
        "display" : "Granulomatous slack skin"
      },
      {
        "code" : "331176",
        "display" : "Severe congenital neutropenia due to G6PC3 deficiency"
      },
      {
        "code" : "331187",
        "display" : "Immunodeficiency due to MASP-2 deficiency"
      },
      {
        "code" : "331190",
        "display" : "Immunodeficiency due to ficolin3 deficiency"
      },
      {
        "code" : "3312",
        "display" : "Thalidomide embryopathy"
      },
      {
        "code" : "331206",
        "display" : "Severe combined immunodeficiency due to complete RAG1/2 deficiency"
      },
      {
        "code" : "331226",
        "display" : "Susceptibility to infection due to TYK2 deficiency"
      },
      {
        "code" : "331235",
        "display" : "Selective IgM deficiency"
      },
      {
        "code" : "3314",
        "display" : "Thiemann disease, familial form"
      },
      {
        "code" : "3316",
        "display" : "Thomas syndrome"
      },
      {
        "code" : "3317",
        "display" : "Thoracolaryngopelvic dysplasia"
      },
      {
        "code" : "3318",
        "display" : "Essential thrombocythemia"
      },
      {
        "code" : "3319",
        "display" : "Congenital amegakaryocytic thrombocytopenia"
      },
      {
        "code" : "332",
        "display" : "Congenital intrinsic factor deficiency"
      },
      {
        "code" : "3320",
        "display" : "Thrombocytopenia-absent radius syndrome"
      },
      {
        "code" : "33208",
        "display" : "Idiopathic hypersomnia"
      },
      {
        "code" : "3322",
        "display" : "Hoyeraal-Hreidarsson syndrome"
      },
      {
        "code" : "33226",
        "display" : "Waldenström macroglobulinemia"
      },
      {
        "code" : "3324",
        "display" : "Familial thrombomodulin anomalies"
      },
      {
        "code" : "3325",
        "display" : "Classic heparin-induced thrombocytopenia"
      },
      {
        "code" : "3326",
        "display" : "Thymic-renal-anal-lung dysplasia"
      },
      {
        "code" : "3327",
        "display" : "Thyrocerebrorenal syndrome"
      },
      {
        "code" : "33276",
        "display" : "Kaposi sarcoma"
      },
      {
        "code" : "3328",
        "display" : "Absent tibia-polydactyly-arachnoid cyst syndrome"
      },
      {
        "code" : "3329",
        "display" : "Tibial aplasia-ectrodactyly syndrome"
      },
      {
        "code" : "333",
        "display" : "Farber disease"
      },
      {
        "code" : "33314",
        "display" : "Jessner lymphocytic infiltration of the skin"
      },
      {
        "code" : "33355",
        "display" : "Reticular dysgenesis"
      },
      {
        "code" : "33364",
        "display" : "Trichothiodystrophy"
      },
      {
        "code" : "3337",
        "display" : "Primary Fanconi renotubular syndrome"
      },
      {
        "code" : "3338",
        "display" : "Toriello-Carey syndrome"
      },
      {
        "code" : "3339",
        "display" : "Oculoectodermal syndrome"
      },
      {
        "code" : "334",
        "display" : "Hereditary atrial fibrillation"
      },
      {
        "code" : "33402",
        "display" : "Pediatric hepatocellular carcinoma"
      },
      {
        "code" : "33408",
        "display" : "Bullous lichen planus"
      },
      {
        "code" : "3341",
        "display" : "Torticollis-keloids-cryptorchidism-renal dysplasia syndrome"
      },
      {
        "code" : "3342",
        "display" : "Arterial tortuosity syndrome"
      },
      {
        "code" : "3343",
        "display" : "Toxocariasis"
      },
      {
        "code" : "3344",
        "display" : "Weismann-Netter syndrome"
      },
      {
        "code" : "33445",
        "display" : "Neuroectodermal melanolysosomal disease"
      },
      {
        "code" : "3346",
        "display" : "Tracheal agenesis"
      },
      {
        "code" : "3347",
        "display" : "Mounier-Kühn syndrome"
      },
      {
        "code" : "33475",
        "display" : "Meningococcal meningitis"
      },
      {
        "code" : "3348",
        "display" : "Tracheobronchopathia osteochondroplastica"
      },
      {
        "code" : "335",
        "display" : "Congenital fibrinogen deficiency"
      },
      {
        "code" : "3350",
        "display" : "Tremor-nystagmus-duodenal ulcer syndrome"
      },
      {
        "code" : "3351",
        "display" : "Trichodental syndrome"
      },
      {
        "code" : "3352",
        "display" : "Tricho-dento-osseous syndrome"
      },
      {
        "code" : "3353",
        "display" : "Trichodermodysplasia-dental alterations syndrome"
      },
      {
        "code" : "33543",
        "display" : "Kleine-Levin syndrome"
      },
      {
        "code" : "3355",
        "display" : "Trichoodontoonychial dysplasia"
      },
      {
        "code" : "33572",
        "display" : "5-oxoprolinase deficiency"
      },
      {
        "code" : "33573",
        "display" : "Gamma-glutamyl transpeptidase deficiency"
      },
      {
        "code" : "33574",
        "display" : "Glutamate-cysteine ligase deficiency"
      },
      {
        "code" : "33577",
        "display" : "Nodular non-suppurative panniculitis"
      },
      {
        "code" : "3361",
        "display" : "Trichodysplasia-xeroderma syndrome"
      },
      {
        "code" : "3363",
        "display" : "Trichomegaly-retina pigmentary degeneration-dwarfism syndrome"
      },
      {
        "code" : "3365",
        "display" : "Trigonocephaly-broad thumbs syndrome"
      },
      {
        "code" : "3366",
        "display" : "Non-syndromic metopic craniosynostosis"
      },
      {
        "code" : "3368",
        "display" : "Trigonocephaly-bifid nose-acral anomalies syndrome"
      },
      {
        "code" : "3369",
        "display" : "Trigonocephaly-short stature-developmental delay syndrome"
      },
      {
        "code" : "337",
        "display" : "Fibrodysplasia ossificans progressiva"
      },
      {
        "code" : "3374",
        "display" : "Unilateral ocular duplication"
      },
      {
        "code" : "3375",
        "display" : "Trisomy X syndrome"
      },
      {
        "code" : "3376",
        "display" : "Triploidy syndrome"
      },
      {
        "code" : "3377",
        "display" : "Trismus-pseudocamptodactyly syndrome"
      },
      {
        "code" : "3378",
        "display" : "Trisomy 13 syndrome"
      },
      {
        "code" : "3379",
        "display" : "Distal duplication 17q syndrome"
      },
      {
        "code" : "3380",
        "display" : "Trisomy 18 syndrome"
      },
      {
        "code" : "3383",
        "display" : "Humerus trochlea aplasia"
      },
      {
        "code" : "3384",
        "display" : "Common arterial trunk"
      },
      {
        "code" : "3385",
        "display" : "African trypanosomiasis"
      },
      {
        "code" : "3386",
        "display" : "American trypanosomiasis"
      },
      {
        "code" : "3387",
        "display" : "Isolated anterior cervical hypertrichosis"
      },
      {
        "code" : "3392",
        "display" : "Tularemia"
      },
      {
        "code" : "340",
        "display" : "Hemorrhagic fever-renal syndrome"
      },
      {
        "code" : "3400",
        "display" : "Aorto-ventricular tunnel"
      },
      {
        "code" : "3402",
        "display" : "Transient tyrosinemia of the newborn"
      },
      {
        "code" : "3403",
        "display" : "Uhl anomaly"
      },
      {
        "code" : "3404",
        "display" : "Ulbright-Hodes syndrome"
      },
      {
        "code" : "3405",
        "display" : "Umbilical cord ulceration-intestinal atresia syndrome"
      },
      {
        "code" : "3406",
        "display" : "Ulerythema ophryogenesis"
      },
      {
        "code" : "3408",
        "display" : "Upington disease"
      },
      {
        "code" : "3409",
        "display" : "Urban-Rogers-Meyer syndrome"
      },
      {
        "code" : "3411",
        "display" : "Double uterus-hemivagina-renal agenesis syndrome"
      },
      {
        "code" : "3412",
        "display" : "VACTERL with hydrocephalus"
      },
      {
        "code" : "34145",
        "display" : "Immunoglobulin A nephropathy"
      },
      {
        "code" : "34149",
        "display" : "Autosomal dominant tubulointerstitial kidney disease"
      },
      {
        "code" : "3416",
        "display" : "Hyperostosis corticalis generalisata"
      },
      {
        "code" : "3417",
        "display" : "Van den Bosch syndrome"
      },
      {
        "code" : "342",
        "display" : "Familial Mediterranean fever"
      },
      {
        "code" : "34217",
        "display" : "Naxos disease"
      },
      {
        "code" : "3424",
        "display" : "Velo-facial-skeletal syndrome"
      },
      {
        "code" : "3426",
        "display" : "Double outlet right ventricle"
      },
      {
        "code" : "3427",
        "display" : "Double outlet left ventricle"
      },
      {
        "code" : "3429",
        "display" : "Verloove Vanhorick-Brubakk syndrome"
      },
      {
        "code" : "343",
        "display" : "Hyperimmunoglobulinemia D with periodic fever"
      },
      {
        "code" : "3433",
        "display" : "Microcephaly-brachydactyly-kyphoscoliosis syndrome"
      },
      {
        "code" : "3434",
        "display" : "MMEP syndrome"
      },
      {
        "code" : "3437",
        "display" : "Vogt-Koyanagi-Harada disease"
      },
      {
        "code" : "3439",
        "display" : "Von Voss-Cherstvoy syndrome"
      },
      {
        "code" : "3440",
        "display" : "Waardenburg syndrome"
      },
      {
        "code" : "3447",
        "display" : "Weaver syndrome"
      },
      {
        "code" : "3448",
        "display" : "Weaver-Williams syndrome"
      },
      {
        "code" : "3449",
        "display" : "Weill-Marchesani syndrome"
      },
      {
        "code" : "345",
        "display" : "Dissecting cellulitis of the scalp"
      },
      {
        "code" : "34514",
        "display" : "Telethonin-related limb-girdle muscular dystrophy R7"
      },
      {
        "code" : "34515",
        "display" : "FKRP-related limb-girdle muscular dystrophy R9"
      },
      {
        "code" : "34516",
        "display" : "DNAJB6-related limb-girdle muscular dystrophy D1"
      },
      {
        "code" : "3452",
        "display" : "Whipple disease"
      },
      {
        "code" : "34520",
        "display" : "Congenital muscular dystrophy with integrin alpha-7 deficiency"
      },
      {
        "code" : "34528",
        "display" : "Autosomal dominant primary hypomagnesemia with hypocalciuria"
      },
      {
        "code" : "3453",
        "display" : "Autoimmune polyendocrinopathy type 1"
      },
      {
        "code" : "3454",
        "display" : "Wieacker-Wolff syndrome"
      },
      {
        "code" : "3455",
        "display" : "Wiedemann-Rautenstrauch syndrome"
      },
      {
        "code" : "3456",
        "display" : "Wildervanck syndrome"
      },
      {
        "code" : "34587",
        "display" : "Danon disease"
      },
      {
        "code" : "3459",
        "display" : "Wilson-Turner syndrome"
      },
      {
        "code" : "34592",
        "display" : "Immunodeficiency by defective expression of MHC class I"
      },
      {
        "code" : "346",
        "display" : "Quinquaud folliculitis decalvans"
      },
      {
        "code" : "3463",
        "display" : "Wolfram syndrome"
      },
      {
        "code" : "3464",
        "display" : "Woodhouse-Sakati syndrome"
      },
      {
        "code" : "3465",
        "display" : "Worster-Drought syndrome"
      },
      {
        "code" : "3466",
        "display" : "WT limb-blood syndrome"
      },
      {
        "code" : "3467",
        "display" : "Hereditary xanthinuria"
      },
      {
        "code" : "3469",
        "display" : "XK aprosencephaly syndrome"
      },
      {
        "code" : "347",
        "display" : "Frasier syndrome"
      },
      {
        "code" : "3471",
        "display" : "Young syndrome"
      },
      {
        "code" : "3472",
        "display" : "Yunis-Varon syndrome"
      },
      {
        "code" : "3473",
        "display" : "Zimmermann-Laband syndrome"
      },
      {
        "code" : "3474",
        "display" : "CHIME syndrome"
      },
      {
        "code" : "348",
        "display" : "Fructose-1,6-bisphosphatase deficiency"
      },
      {
        "code" : "349",
        "display" : "Fucosidosis"
      },
      {
        "code" : "35",
        "display" : "Propionic acidemia"
      },
      {
        "code" : "35062",
        "display" : "Severe disseminated cytomegalovirus infection in immunocompetent patients"
      },
      {
        "code" : "35063",
        "display" : "Fulminant viral hepatitis"
      },
      {
        "code" : "35069",
        "display" : "Infantile neuroaxonal dystrophy"
      },
      {
        "code" : "35078",
        "display" : "T-B+ severe combined immunodeficiency due to JAK3 deficiency"
      },
      {
        "code" : "35093",
        "display" : "Non-syndromic sagittal craniosynostosis"
      },
      {
        "code" : "35099",
        "display" : "Non-syndromic bicoronal craniosynostosis"
      },
      {
        "code" : "351",
        "display" : "Galactosialidosis"
      },
      {
        "code" : "35107",
        "display" : "Desmosterolosis"
      },
      {
        "code" : "35120",
        "display" : "Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency"
      },
      {
        "code" : "35121",
        "display" : "Lysosomal acid phosphatase deficiency"
      },
      {
        "code" : "35122",
        "display" : "Congenital sucrase-isomaltase deficiency"
      },
      {
        "code" : "35125",
        "display" : "Epidermal nevus syndrome"
      },
      {
        "code" : "35173",
        "display" : "X-linked dominant chondrodysplasia punctata"
      },
      {
        "code" : "352328",
        "display" : "MEGDEL syndrome"
      },
      {
        "code" : "352333",
        "display" : "Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome"
      },
      {
        "code" : "352403",
        "display" : "Spectrin-associated autosomal recessive cerebellar ataxia"
      },
      {
        "code" : "352447",
        "display" : "Progressive external ophthalmoplegia-myopathy-emaciation syndrome"
      },
      {
        "code" : "352470",
        "display" : "DNA2-related mitochondrial DNA deletion syndrome"
      },
      {
        "code" : "352479",
        "display" : "ISPD-related limb-girdle muscular dystrophy R20"
      },
      {
        "code" : "352490",
        "display" : "Autism spectrum disorder due to AUTS2 deficiency"
      },
      {
        "code" : "352530",
        "display" : "Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome"
      },
      {
        "code" : "352540",
        "display" : "Oncogenic osteomalacia"
      },
      {
        "code" : "352563",
        "display" : "Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency"
      },
      {
        "code" : "352577",
        "display" : "Bainbridge-Ropers syndrome"
      },
      {
        "code" : "352582",
        "display" : "Familial infantile myoclonic epilepsy"
      },
      {
        "code" : "352587",
        "display" : "Focal epilepsy-intellectual disability-cerebro-cerebellar malformation"
      },
      {
        "code" : "352596",
        "display" : "Progressive myoclonic epilepsy with dystonia"
      },
      {
        "code" : "352629",
        "display" : "16q24.1 microdeletion syndrome"
      },
      {
        "code" : "352636",
        "display" : "Phalangeal microgeodic syndrome"
      },
      {
        "code" : "352641",
        "display" : "Autosomal recessive cerebellar ataxia with late-onset spasticity"
      },
      {
        "code" : "352649",
        "display" : "Brain dopamine-serotonin vesicular transport disease"
      },
      {
        "code" : "352654",
        "display" : "Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome"
      },
      {
        "code" : "352657",
        "display" : "Hereditary benign intraepithelial dyskeratosis"
      },
      {
        "code" : "352662",
        "display" : "Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome"
      },
      {
        "code" : "352665",
        "display" : "Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion"
      },
      {
        "code" : "352670",
        "display" : "Autosomal dominant intermediate Charcot-Marie-Tooth disease type F"
      },
      {
        "code" : "352675",
        "display" : "X-linked Charcot-Marie-Tooth disease type 6"
      },
      {
        "code" : "352682",
        "display" : "Cobblestone lissencephaly without muscular or ocular involvement"
      },
      {
        "code" : "352709",
        "display" : "CLN13 disease"
      },
      {
        "code" : "352712",
        "display" : "Facial dysmorphism-immunodeficiency-livedo-short stature syndrome"
      },
      {
        "code" : "352718",
        "display" : "Progressive retinal dystrophy due to retinol transport defect"
      },
      {
        "code" : "352723",
        "display" : "Attenuated Chédiak-Higashi syndrome"
      },
      {
        "code" : "352731",
        "display" : "Oculocutaneous albinism type 1"
      },
      {
        "code" : "352734",
        "display" : "Minimal pigment oculocutaneous albinism type 1"
      },
      {
        "code" : "352737",
        "display" : "Temperature-sensitive oculocutaneous albinism type 1"
      },
      {
        "code" : "352745",
        "display" : "Oculocutaneous albinism type 7"
      },
      {
        "code" : "352763",
        "display" : "Scleredema"
      },
      {
        "code" : "353",
        "display" : "Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5"
      },
      {
        "code" : "353217",
        "display" : "Epileptic encephalopathy with global cerebral demyelination"
      },
      {
        "code" : "353220",
        "display" : "Familial primary localized cutaneous amyloidosis"
      },
      {
        "code" : "353253",
        "display" : "Burning mouth syndrome"
      },
      {
        "code" : "353277",
        "display" : "Rubinstein-Taybi syndrome due to CREBBP mutations"
      },
      {
        "code" : "353281",
        "display" : "Rubinstein-Taybi syndrome due to 16p13.3 microdeletion"
      },
      {
        "code" : "353284",
        "display" : "Rubinstein-Taybi syndrome due to EP300 haploinsufficiency"
      },
      {
        "code" : "353298",
        "display" : "Roifman syndrome"
      },
      {
        "code" : "353308",
        "display" : "Pyruvate carboxylase deficiency, infantile type"
      },
      {
        "code" : "353314",
        "display" : "Pyruvate carboxylase deficiency, severe neonatal type"
      },
      {
        "code" : "353320",
        "display" : "Pyruvate carboxylase deficiency, benign type"
      },
      {
        "code" : "353327",
        "display" : "Congenital myasthenic syndromes with glycosylation defect"
      },
      {
        "code" : "353334",
        "display" : "Congenital retinal arteriovenous communication"
      },
      {
        "code" : "353344",
        "display" : "Idiopathic macular telangiectasia type 1"
      },
      {
        "code" : "353351",
        "display" : "Idiopathic macular telangiectasia type 3"
      },
      {
        "code" : "353356",
        "display" : "Vasoproliferative tumor of the retina"
      },
      {
        "code" : "354",
        "display" : "GM1 gangliosidosis"
      },
      {
        "code" : "355",
        "display" : "Gaucher disease"
      },
      {
        "code" : "356",
        "display" : "Gerstmann-Straussler-Scheinker syndrome"
      },
      {
        "code" : "35612",
        "display" : "Nanophthalmos"
      },
      {
        "code" : "35664",
        "display" : "ALDH18A1-related De Barsy syndrome"
      },
      {
        "code" : "35686",
        "display" : "Serpiginous choroiditis"
      },
      {
        "code" : "35687",
        "display" : "Erdheim-Chester disease"
      },
      {
        "code" : "35689",
        "display" : "Primary lateral sclerosis"
      },
      {
        "code" : "356961",
        "display" : "SLC35A2-CDG"
      },
      {
        "code" : "356978",
        "display" : "D,L-2-hydroxyglutaric aciduria"
      },
      {
        "code" : "356996",
        "display" : "ANK3-related intellectual disability-sleep disturbance syndrome"
      },
      {
        "code" : "357001",
        "display" : "19p13.13 microdeletion syndrome"
      },
      {
        "code" : "357008",
        "display" : "Hemolytic uremic syndrome with DGKE deficiency"
      },
      {
        "code" : "35701",
        "display" : "3-hydroxy-3-methylglutaryl-CoA synthase deficiency"
      },
      {
        "code" : "357027",
        "display" : "Hereditary retinoblastoma"
      },
      {
        "code" : "357034",
        "display" : "Non-hereditary retinoblastoma"
      },
      {
        "code" : "35704",
        "display" : "L-Arginine:glycine amidinotransferase deficiency"
      },
      {
        "code" : "357043",
        "display" : "Amyotrophic lateral sclerosis type 4"
      },
      {
        "code" : "357058",
        "display" : "Autosomal recessive cutis laxa type 2A"
      },
      {
        "code" : "35706",
        "display" : "Glutaric acidemia type 3"
      },
      {
        "code" : "357064",
        "display" : "Autosomal recessive cutis laxa type 2B"
      },
      {
        "code" : "357074",
        "display" : "Autosomal recessive cutis laxa type 2, classic type"
      },
      {
        "code" : "35708",
        "display" : "Aromatic L-amino acid decarboxylase deficiency"
      },
      {
        "code" : "35710",
        "display" : "Glucose-galactose malabsorption"
      },
      {
        "code" : "357107",
        "display" : "Arterial thoracic outlet syndrome"
      },
      {
        "code" : "357131",
        "display" : "Venous thoracic outlet syndrome"
      },
      {
        "code" : "357154",
        "display" : "Oral submucous fibrosis"
      },
      {
        "code" : "357158",
        "display" : "Mandibulofacial dysostosis-macroblepharon-macrostomia syndrome"
      },
      {
        "code" : "357175",
        "display" : "Short ulna-dysmorphism-hypotonia-intellectual disability syndrome"
      },
      {
        "code" : "357220",
        "display" : "Primary essential cutis verticis gyrata"
      },
      {
        "code" : "357225",
        "display" : "Primary non-essential cutis verticis gyrata"
      },
      {
        "code" : "357237",
        "display" : "Combined immunodeficiency due to CARD11 deficiency"
      },
      {
        "code" : "357329",
        "display" : "Combined immunodeficiency due to IL21R deficiency"
      },
      {
        "code" : "357332",
        "display" : "Syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome"
      },
      {
        "code" : "35737",
        "display" : "Morning glory disc anomaly"
      },
      {
        "code" : "358",
        "display" : "Gitelman syndrome"
      },
      {
        "code" : "35858",
        "display" : "Imerslund-Gräsbeck syndrome"
      },
      {
        "code" : "35878",
        "display" : "Hyperinsulinism-hyperammonemia syndrome"
      },
      {
        "code" : "35889",
        "display" : "Acute opioid intoxication"
      },
      {
        "code" : "35909",
        "display" : "Combined deficiency of factor V and factor VIII"
      },
      {
        "code" : "36",
        "display" : "Acrocallosal syndrome"
      },
      {
        "code" : "360",
        "display" : "Glioblastoma"
      },
      {
        "code" : "361",
        "display" : "Familial glucocorticoid deficiency"
      },
      {
        "code" : "36234",
        "display" : "Bacterial toxic-shock syndrome"
      },
      {
        "code" : "36235",
        "display" : "Staphylococcal scarlet fever"
      },
      {
        "code" : "36236",
        "display" : "Staphylococcal scalded skin syndrome"
      },
      {
        "code" : "36237",
        "display" : "Bullous impetigo"
      },
      {
        "code" : "36238",
        "display" : "Staphylococcal necrotizing pneumonia"
      },
      {
        "code" : "36258",
        "display" : "Buerger disease"
      },
      {
        "code" : "36273",
        "display" : "Gastric linitis plastica"
      },
      {
        "code" : "363396",
        "display" : "High myopia-sensorineural deafness syndrome"
      },
      {
        "code" : "363400",
        "display" : "Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome"
      },
      {
        "code" : "363409",
        "display" : "Fetal akinesia-cerebral and retinal hemorrhage syndrome"
      },
      {
        "code" : "363412",
        "display" : "Hypomyelination with brain stem and spinal cord involvement and leg spasticity"
      },
      {
        "code" : "363417",
        "display" : "Temtamy preaxial brachydactyly syndrome"
      },
      {
        "code" : "363424",
        "display" : "Multiple mitochondrial dysfunctions syndrome type 3"
      },
      {
        "code" : "363429",
        "display" : "Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome"
      },
      {
        "code" : "363432",
        "display" : "Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency"
      },
      {
        "code" : "363444",
        "display" : "THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome"
      },
      {
        "code" : "363447",
        "display" : "Autosomal dominant childhood-onset proximal spinal muscular atrophy"
      },
      {
        "code" : "363454",
        "display" : "BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy"
      },
      {
        "code" : "363478",
        "display" : "Paratesticular adenocarcinoma"
      },
      {
        "code" : "363483",
        "display" : "Testicular teratoma"
      },
      {
        "code" : "363489",
        "display" : "Sex cord-stromal tumor of testis"
      },
      {
        "code" : "363494",
        "display" : "Non-seminomatous germ cell tumor of testis"
      },
      {
        "code" : "363523",
        "display" : "Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome"
      },
      {
        "code" : "363528",
        "display" : "Intellectual disability-strabismus syndrome"
      },
      {
        "code" : "363534",
        "display" : "Mitochondrial DNA depletion syndrome, hepatocerebrorenal form"
      },
      {
        "code" : "363540",
        "display" : "Leukoencephalopathy with mild cerebellar ataxia and white matter edema"
      },
      {
        "code" : "363549",
        "display" : "Acute encephalopathy with biphasic seizures and late reduced diffusion"
      },
      {
        "code" : "36355",
        "display" : "Bleeding disorder due to P2Y12 defect"
      },
      {
        "code" : "363558",
        "display" : "New-onset refractory status epilepticus"
      },
      {
        "code" : "363611",
        "display" : "CTCF-related neurodevelopmental disorder"
      },
      {
        "code" : "363618",
        "display" : "LMNA-related cardiocutaneous progeria syndrome"
      },
      {
        "code" : "363623",
        "display" : "GMPPB-related limb-girdle muscular dystrophy R19"
      },
      {
        "code" : "363649",
        "display" : "Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome"
      },
      {
        "code" : "363654",
        "display" : "X-linked parkinsonism-spasticity syndrome"
      },
      {
        "code" : "363659",
        "display" : "20q11.2 microduplication syndrome"
      },
      {
        "code" : "363665",
        "display" : "Acroosteolysis-keloid-like lesions-premature aging syndrome"
      },
      {
        "code" : "36367",
        "display" : "Distal deletion 1q syndrome"
      },
      {
        "code" : "363677",
        "display" : "Childhood-onset autosomal recessive myopathy with external ophthalmoplegia"
      },
      {
        "code" : "363680",
        "display" : "2p13.2 microdeletion syndrome"
      },
      {
        "code" : "363686",
        "display" : "Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome"
      },
      {
        "code" : "363694",
        "display" : "Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome"
      },
      {
        "code" : "363700",
        "display" : "Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion"
      },
      {
        "code" : "363705",
        "display" : "Craniofaciofrontodigital syndrome"
      },
      {
        "code" : "363710",
        "display" : "Spinocerebellar ataxia type 37"
      },
      {
        "code" : "363717",
        "display" : "Alexander disease type I"
      },
      {
        "code" : "363722",
        "display" : "Alexander disease type II"
      },
      {
        "code" : "363727",
        "display" : "X-linked dyserythropoietic anemia with abnormal platelets and neutropenia"
      },
      {
        "code" : "363741",
        "display" : "Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome"
      },
      {
        "code" : "363746",
        "display" : "Balint syndrome"
      },
      {
        "code" : "36383",
        "display" : "COL4A1/2-related familial vascular leukoencephalopathy"
      },
      {
        "code" : "36386",
        "display" : "Hereditary sensory and autonomic neuropathy type 1"
      },
      {
        "code" : "36387",
        "display" : "Genetic epilepsy with febrile seizure plus"
      },
      {
        "code" : "363958",
        "display" : "17q21.31 microdeletion syndrome"
      },
      {
        "code" : "363965",
        "display" : "Koolen-De Vries syndrome due to a point mutation"
      },
      {
        "code" : "363969",
        "display" : "Autosomal recessive cerebral atrophy"
      },
      {
        "code" : "36397",
        "display" : "Adiposis dolorosa"
      },
      {
        "code" : "363972",
        "display" : "Noonan syndrome-like disorder with juvenile myelomonocytic leukemia"
      },
      {
        "code" : "363976",
        "display" : "Giant cell tumor of bone"
      },
      {
        "code" : "363981",
        "display" : "Charcot-Marie-Tooth disease type 4B3"
      },
      {
        "code" : "363989",
        "display" : "Familial benign flecked retina"
      },
      {
        "code" : "363992",
        "display" : "Ichthyosis-short stature-brachydactyly-microspherophakia syndrome"
      },
      {
        "code" : "363999",
        "display" : "Non-immune hydrops fetalis"
      },
      {
        "code" : "364",
        "display" : "Glycogen storage disease due to glucose-6-phosphatase deficiency"
      },
      {
        "code" : "364013",
        "display" : "Immune hydrops fetalis"
      },
      {
        "code" : "364028",
        "display" : "X-linked intellectual disability due to GRIA3 mutations"
      },
      {
        "code" : "364033",
        "display" : "Systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood"
      },
      {
        "code" : "364039",
        "display" : "Hydroa vacciniforme-like lymphoma"
      },
      {
        "code" : "364043",
        "display" : "ALK-positive large B-cell lymphoma"
      },
      {
        "code" : "364055",
        "display" : "Severe early-childhood-onset retinal dystrophy"
      },
      {
        "code" : "364063",
        "display" : "Infantile epileptic-dyskinetic encephalopathy"
      },
      {
        "code" : "36412",
        "display" : "Hypocomplementemic urticarial vasculitis"
      },
      {
        "code" : "364198",
        "display" : "Bipartite talus"
      },
      {
        "code" : "36426",
        "display" : "Stevens-Johnson syndrome"
      },
      {
        "code" : "364577",
        "display" : "Intellectual disability-brachydactyly-Pierre Robin syndrome"
      },
      {
        "code" : "365",
        "display" : "Glycogen storage disease due to acid maltase deficiency"
      },
      {
        "code" : "366",
        "display" : "Glycogen storage disease due to glycogen debranching enzyme deficiency"
      },
      {
        "code" : "367",
        "display" : "Glycogen storage disease due to glycogen branching enzyme deficiency"
      },
      {
        "code" : "368",
        "display" : "Glycogen storage disease due to muscle glycogen phosphorylase deficiency"
      },
      {
        "code" : "36899",
        "display" : "Myoclonus-dystonia syndrome"
      },
      {
        "code" : "369",
        "display" : "Glycogen storage disease due to liver glycogen phosphorylase deficiency"
      },
      {
        "code" : "36913",
        "display" : "Autoimmune hypoparathyroidism"
      },
      {
        "code" : "369837",
        "display" : "Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome"
      },
      {
        "code" : "369840",
        "display" : "TRAPPC11-related limb-girdle muscular dystrophy R18"
      },
      {
        "code" : "369847",
        "display" : "Intellectual disability-hyperkinetic movement-truncal ataxia syndrome"
      },
      {
        "code" : "369852",
        "display" : "Congenital neutropenia-myelofibrosis-nephromegaly syndrome"
      },
      {
        "code" : "369861",
        "display" : "Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome"
      },
      {
        "code" : "369867",
        "display" : "Autosomal recessive intermediate Charcot-Marie-Tooth disease type C"
      },
      {
        "code" : "369873",
        "display" : "Obesity due to SIM1 deficiency"
      },
      {
        "code" : "369881",
        "display" : "2p21 microdeletion syndrome without cystinuria"
      },
      {
        "code" : "369891",
        "display" : "Developmental delay-facial dysmorphism syndrome due to MED13L deficiency"
      },
      {
        "code" : "369897",
        "display" : "Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies"
      },
      {
        "code" : "369913",
        "display" : "Combined oxidative phosphorylation defect type 17"
      },
      {
        "code" : "369920",
        "display" : "Pontocerebellar hypoplasia type 9"
      },
      {
        "code" : "369929",
        "display" : "Primary hyperaldosteronism-seizures-neurological abnormalities syndrome"
      },
      {
        "code" : "369939",
        "display" : "Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome"
      },
      {
        "code" : "369942",
        "display" : "CADDS"
      },
      {
        "code" : "369950",
        "display" : "Intellectual disability-seizures-macrocephaly-obesity syndrome"
      },
      {
        "code" : "369955",
        "display" : "Methylmalonic acidemia with homocystinuria, type cblJ"
      },
      {
        "code" : "369962",
        "display" : "Methylmalonic acidemia with homocystinuria, type cblX"
      },
      {
        "code" : "369970",
        "display" : "Microcornea-myopic chorioretinal atrophy-telecanthus syndrome"
      },
      {
        "code" : "369979",
        "display" : "Finger hyperphalangy-toe anomalies-severe pectus excavatum syndrome"
      },
      {
        "code" : "369992",
        "display" : "Severe dermatitis-multiple allergies-metabolic wasting syndrome"
      },
      {
        "code" : "369999",
        "display" : "Diffuse palmoplantar keratoderma with painful fissures"
      },
      {
        "code" : "37",
        "display" : "Acrodermatitis enteropathica"
      },
      {
        "code" : "370002",
        "display" : "Focal palmoplantar keratoderma with joint keratoses"
      },
      {
        "code" : "370010",
        "display" : "Intellectual disability-facial dysmorphism-hand anomalies syndrome"
      },
      {
        "code" : "370015",
        "display" : "Spondyloepimetaphyseal dysplasia, Isidor-Toutain type"
      },
      {
        "code" : "370022",
        "display" : "Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome"
      },
      {
        "code" : "370026",
        "display" : "Acute myeloid leukemia with t(8;16)(p11;p13) translocation"
      },
      {
        "code" : "370034",
        "display" : "Familial syringomyelia"
      },
      {
        "code" : "370039",
        "display" : "Angora hair nevus"
      },
      {
        "code" : "370046",
        "display" : "Didymosis aplasticosebacea"
      },
      {
        "code" : "370052",
        "display" : "SCALP syndrome"
      },
      {
        "code" : "370059",
        "display" : "NEVADA syndrome"
      },
      {
        "code" : "370076",
        "display" : "Fetal carbamazepine syndrome"
      },
      {
        "code" : "370079",
        "display" : "Proximal 16p11.2 microduplication syndrome"
      },
      {
        "code" : "370088",
        "display" : "Acute infantile liver failure-multisystemic involvement syndrome"
      },
      {
        "code" : "370091",
        "display" : "Oculocutaneous albinism type 5"
      },
      {
        "code" : "370097",
        "display" : "Oculocutaneous albinism type 6"
      },
      {
        "code" : "370103",
        "display" : "Primary dystonia, DYT17 type"
      },
      {
        "code" : "370109",
        "display" : "Ataxia-telangiectasia variant"
      },
      {
        "code" : "370127",
        "display" : "Medich giant platelet syndrome"
      },
      {
        "code" : "370131",
        "display" : "White platelet syndrome"
      },
      {
        "code" : "370334",
        "display" : "Extraskeletal Ewing sarcoma"
      },
      {
        "code" : "370348",
        "display" : "Peripheral primitive neuroectodermal tumor"
      },
      {
        "code" : "370396",
        "display" : "Small cell carcinoma of the ovary"
      },
      {
        "code" : "37042",
        "display" : "Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome"
      },
      {
        "code" : "370921",
        "display" : "STT3A-CDG"
      },
      {
        "code" : "370924",
        "display" : "STT3B-CDG"
      },
      {
        "code" : "370927",
        "display" : "SSR4-CDG"
      },
      {
        "code" : "370930",
        "display" : "XYLT1-CDG"
      },
      {
        "code" : "370933",
        "display" : "GM3 synthase deficiency"
      },
      {
        "code" : "370943",
        "display" : "Autism spectrum disorder-epilepsy-arthrogryposis syndrome"
      },
      {
        "code" : "370959",
        "display" : "Congenital muscular dystrophy with cerebellar involvement"
      },
      {
        "code" : "370968",
        "display" : "Congenital muscular dystrophy with intellectual disability"
      },
      {
        "code" : "370980",
        "display" : "Congenital muscular dystrophy without intellectual disability"
      },
      {
        "code" : "370997",
        "display" : "Muscle-eye-brain disease with bilateral multicystic leucodystrophy"
      },
      {
        "code" : "371",
        "display" : "Glycogen storage disease due to muscle phosphofructokinase deficiency"
      },
      {
        "code" : "371007",
        "display" : "Congenital muscular dystrophy with hyperlaxity"
      },
      {
        "code" : "371364",
        "display" : "Hypotonia-speech impairment-severe cognitive delay syndrome"
      },
      {
        "code" : "371428",
        "display" : "Multicentric osteolysis-nodulosis-arthropathy spectrum"
      },
      {
        "code" : "37202",
        "display" : "Interstitial cystitis"
      },
      {
        "code" : "373",
        "display" : "Simpson-Golabi-Behmel syndrome"
      },
      {
        "code" : "375",
        "display" : "Anti-glomerular basement membrane disease"
      },
      {
        "code" : "37553",
        "display" : "Andersen-Tawil syndrome"
      },
      {
        "code" : "37559",
        "display" : "Acquired kinky hair syndrome"
      },
      {
        "code" : "376",
        "display" : "Gordon syndrome"
      },
      {
        "code" : "37612",
        "display" : "Episodic ataxia type 1"
      },
      {
        "code" : "377",
        "display" : "Gorlin syndrome"
      },
      {
        "code" : "37748",
        "display" : "Schnitzler syndrome"
      },
      {
        "code" : "379",
        "display" : "Chronic granulomatous disease"
      },
      {
        "code" : "38",
        "display" : "Acrokeratoelastoidosis of Costa"
      },
      {
        "code" : "380",
        "display" : "Greig cephalopolysyndactyly syndrome"
      },
      {
        "code" : "381",
        "display" : "Griscelli syndrome"
      },
      {
        "code" : "382",
        "display" : "Guanidinoacetate methyltransferase deficiency"
      },
      {
        "code" : "384",
        "display" : "Huriez syndrome"
      },
      {
        "code" : "386",
        "display" : "Hepatic cystic hamartoma"
      },
      {
        "code" : "388",
        "display" : "Hirschsprung disease"
      },
      {
        "code" : "38874",
        "display" : "Dihydropyrimidinuria"
      },
      {
        "code" : "389",
        "display" : "Langerhans cell histiocytosis"
      },
      {
        "code" : "39",
        "display" : "Acromelanosis"
      },
      {
        "code" : "390",
        "display" : "Histoplasmosis"
      },
      {
        "code" : "39041",
        "display" : "Omenn syndrome"
      },
      {
        "code" : "39044",
        "display" : "Uveal melanoma"
      },
      {
        "code" : "391",
        "display" : "Classic Hodgkin lymphoma"
      },
      {
        "code" : "391307",
        "display" : "Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome"
      },
      {
        "code" : "391311",
        "display" : "Susceptibility to viral and mycobacterial infections due to STAT1 deficiency"
      },
      {
        "code" : "391316",
        "display" : "Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression"
      },
      {
        "code" : "391320",
        "display" : "East Texas bleeding disorder"
      },
      {
        "code" : "391327",
        "display" : "X-linked calvarial hyperostosis"
      },
      {
        "code" : "391330",
        "display" : "X-linked osteoporosis with fractures"
      },
      {
        "code" : "391343",
        "display" : "Fatal post-viral neurodegenerative disorder"
      },
      {
        "code" : "391348",
        "display" : "Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome"
      },
      {
        "code" : "391351",
        "display" : "SURF1-related Charcot-Marie-Tooth disease type 4"
      },
      {
        "code" : "391366",
        "display" : "Growth retardation-mild developmental delay-chronic hepatitis syndrome"
      },
      {
        "code" : "391372",
        "display" : "FOXP1 Syndrome"
      },
      {
        "code" : "391376",
        "display" : "Congenital microcephaly-severe encephalopathy-progressive cerebral atrophy syndrome"
      },
      {
        "code" : "391384",
        "display" : "Familial episodic pain syndrome"
      },
      {
        "code" : "391389",
        "display" : "Familial episodic pain syndrome with predominantly upper body involvement"
      },
      {
        "code" : "391392",
        "display" : "Familial episodic pain syndrome with predominantly lower limb involvement"
      },
      {
        "code" : "391397",
        "display" : "Hereditary sensory and autonomic neuropathy type 7"
      },
      {
        "code" : "391408",
        "display" : "Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome"
      },
      {
        "code" : "391411",
        "display" : "Atypical juvenile parkinsonism"
      },
      {
        "code" : "391417",
        "display" : "HSD10 disease"
      },
      {
        "code" : "391428",
        "display" : "HSD10 disease, infantile type"
      },
      {
        "code" : "391457",
        "display" : "HSD10 disease, neonatal type"
      },
      {
        "code" : "391474",
        "display" : "Frontorhiny"
      },
      {
        "code" : "391487",
        "display" : "STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome"
      },
      {
        "code" : "391490",
        "display" : "Adult-onset myasthenia gravis"
      },
      {
        "code" : "391497",
        "display" : "Juvenile myasthenia gravis"
      },
      {
        "code" : "391504",
        "display" : "Transient neonatal myasthenia gravis"
      },
      {
        "code" : "391641",
        "display" : "Feingold syndrome type 1"
      },
      {
        "code" : "391646",
        "display" : "Feingold syndrome type 2"
      },
      {
        "code" : "391651",
        "display" : "Glomus tumor"
      },
      {
        "code" : "391655",
        "display" : "Off-periods in Parkinson disease not responding to oral treatment"
      },
      {
        "code" : "391665",
        "display" : "Homozygous familial hypercholesterolemia"
      },
      {
        "code" : "391673",
        "display" : "Necrotizing enterocolitis"
      },
      {
        "code" : "391677",
        "display" : "Short stature-optic atrophy-Pelger-Huët anomaly syndrome"
      },
      {
        "code" : "391723",
        "display" : "Mucinous adenocarcinoma of the appendix"
      },
      {
        "code" : "392",
        "display" : "Holt-Oram syndrome"
      },
      {
        "code" : "393",
        "display" : "46,XX testicular difference of sex development"
      },
      {
        "code" : "394",
        "display" : "Homocystinuria due to cystathionine beta-synthase deficiency"
      },
      {
        "code" : "394529",
        "display" : "Multiple acyl-CoA dehydrogenase deficiency, severe neonatal type"
      },
      {
        "code" : "394532",
        "display" : "Multiple acyl-CoA dehydrogenase deficiency, mild type"
      },
      {
        "code" : "395",
        "display" : "Homocystinuria due to methylene tetrahydrofolate reductase deficiency"
      },
      {
        "code" : "396",
        "display" : "Chronic hiccup"
      },
      {
        "code" : "397",
        "display" : "Giant cell arteritis"
      },
      {
        "code" : "397587",
        "display" : "Deep dermatophytosis"
      },
      {
        "code" : "397590",
        "display" : "Silver-Russell syndrome due to a point mutation"
      },
      {
        "code" : "397593",
        "display" : "Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency"
      },
      {
        "code" : "397606",
        "display" : "PrP systemic amyloidosis"
      },
      {
        "code" : "397612",
        "display" : "Macrocephaly-developmental delay syndrome"
      },
      {
        "code" : "397615",
        "display" : "Obesity due to CEP19 deficiency"
      },
      {
        "code" : "397618",
        "display" : "Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome"
      },
      {
        "code" : "397623",
        "display" : "Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome"
      },
      {
        "code" : "397685",
        "display" : "Familial hyperprolactinemia"
      },
      {
        "code" : "397692",
        "display" : "Hereditary isolated aplastic anemia"
      },
      {
        "code" : "397709",
        "display" : "Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome"
      },
      {
        "code" : "397715",
        "display" : "Joubert syndrome with Jeune asphyxiating thoracic dystrophy"
      },
      {
        "code" : "397725",
        "display" : "COASY protein-associated neurodegeneration"
      },
      {
        "code" : "397735",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2U"
      },
      {
        "code" : "397744",
        "display" : "Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome"
      },
      {
        "code" : "397750",
        "display" : "Periodic paralysis with later-onset distal motor neuropathy"
      },
      {
        "code" : "397755",
        "display" : "Periodic paralysis with transient compartment-like syndrome"
      },
      {
        "code" : "397758",
        "display" : "Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies"
      },
      {
        "code" : "397787",
        "display" : "Combined immunodeficiency due to IKBKB deficiency"
      },
      {
        "code" : "397922",
        "display" : "Ferro-cerebro-cutaneous syndrome"
      },
      {
        "code" : "397927",
        "display" : "Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome"
      },
      {
        "code" : "397933",
        "display" : "Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome"
      },
      {
        "code" : "397937",
        "display" : "Polyglucosan body myopathy type 1"
      },
      {
        "code" : "397941",
        "display" : "MAN1B1-CDG"
      },
      {
        "code" : "397946",
        "display" : "Autosomal spastic paraplegia type 58"
      },
      {
        "code" : "397951",
        "display" : "Microcephaly-thin corpus callosum-intellectual disability syndrome"
      },
      {
        "code" : "397959",
        "display" : "TCR-alpha-beta-positive T-cell deficiency"
      },
      {
        "code" : "397964",
        "display" : "Combined immunodeficiency due to MALT1 deficiency"
      },
      {
        "code" : "397968",
        "display" : "Charcot-Marie-Tooth disease type 2R"
      },
      {
        "code" : "397973",
        "display" : "Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome"
      },
      {
        "code" : "398053",
        "display" : "Adenocarcinoma of the penis"
      },
      {
        "code" : "398058",
        "display" : "Squamous cell carcinoma of the penis"
      },
      {
        "code" : "398063",
        "display" : "Refractory celiac disease"
      },
      {
        "code" : "398069",
        "display" : "Schaaf-Yang syndrome"
      },
      {
        "code" : "398079",
        "display" : "SIM1-related Prader-Willi-like syndrome"
      },
      {
        "code" : "398088",
        "display" : "Hereditary cryohydrocytosis with normal stomatin"
      },
      {
        "code" : "398097",
        "display" : "Neonatal antiphospholipid syndrome"
      },
      {
        "code" : "398109",
        "display" : "Neonatal autoimmune hemolytic anemia"
      },
      {
        "code" : "398117",
        "display" : "Neonatal dermatomyositis"
      },
      {
        "code" : "39812",
        "display" : "Graft versus host disease"
      },
      {
        "code" : "398124",
        "display" : "Neonatal lupus erythematosus"
      },
      {
        "code" : "398127",
        "display" : "Neonatal scleroderma"
      },
      {
        "code" : "398147",
        "display" : "Persistent idiopathic facial pain"
      },
      {
        "code" : "398156",
        "display" : "Oculoauriculofrontonasal syndrome"
      },
      {
        "code" : "398166",
        "display" : "Focal facial dermal dysplasia"
      },
      {
        "code" : "398173",
        "display" : "Focal facial dermal dysplasia type II"
      },
      {
        "code" : "398189",
        "display" : "Focal facial dermal dysplasia type IV"
      },
      {
        "code" : "398961",
        "display" : "Mucinous adenocarcinoma of ovary"
      },
      {
        "code" : "398971",
        "display" : "Clear cell adenocarcinoma of the ovary"
      },
      {
        "code" : "398987",
        "display" : "Malignant teratoma of ovary"
      },
      {
        "code" : "399",
        "display" : "Huntington disease"
      },
      {
        "code" : "399058",
        "display" : "Alpha-B crystallin-related late-onset myopathy"
      },
      {
        "code" : "399081",
        "display" : "KLHL9-related early-onset distal myopathy"
      },
      {
        "code" : "399086",
        "display" : "HNRNPA1-related adult-onset distal myopathy"
      },
      {
        "code" : "399096",
        "display" : "Distal anoctaminopathy"
      },
      {
        "code" : "399103",
        "display" : "Distal nebulin myopathy"
      },
      {
        "code" : "399175",
        "display" : "Traumatic avascular necrosis"
      },
      {
        "code" : "399180",
        "display" : "Secondary non-traumatic avascular necrosis"
      },
      {
        "code" : "399293",
        "display" : "Osteonecrosis of the jaw"
      },
      {
        "code" : "399307",
        "display" : "Idiopathic avascular necrosis"
      },
      {
        "code" : "399329",
        "display" : "Epiphysiolysis of the hip"
      },
      {
        "code" : "399805",
        "display" : "Male infertility with azoospermia or oligozoospermia due to single gene mutation"
      },
      {
        "code" : "399808",
        "display" : "Male infertility with teratozoospermia due to single gene mutation"
      },
      {
        "code" : "40",
        "display" : "Acromesomelic dysplasia, Maroteaux type"
      },
      {
        "code" : "400",
        "display" : "Cystic echinococcosis"
      },
      {
        "code" : "401",
        "display" : "Hymenolepiasis"
      },
      {
        "code" : "401764",
        "display" : "Pancytopenia-developmental delay syndrome"
      },
      {
        "code" : "401768",
        "display" : "Proximal myopathy with extrapyramidal signs"
      },
      {
        "code" : "401777",
        "display" : "Optic atrophy-intellectual disability syndrome"
      },
      {
        "code" : "401780",
        "display" : "Autosomal recessive spastic paraplegia type 61"
      },
      {
        "code" : "401785",
        "display" : "Autosomal recessive spastic paraplegia type 62"
      },
      {
        "code" : "401795",
        "display" : "Autosomal recessive spastic paraplegia type 59"
      },
      {
        "code" : "401800",
        "display" : "Autosomal recessive spastic paraplegia type 60"
      },
      {
        "code" : "401805",
        "display" : "Autosomal recessive spastic paraplegia type 63"
      },
      {
        "code" : "401810",
        "display" : "Autosomal recessive spastic paraplegia type 64"
      },
      {
        "code" : "401815",
        "display" : "Autosomal recessive spastic paraplegia type 66"
      },
      {
        "code" : "401820",
        "display" : "Autosomal recessive spastic paraplegia type 67"
      },
      {
        "code" : "401830",
        "display" : "Autosomal recessive spastic paraplegia type 69"
      },
      {
        "code" : "401835",
        "display" : "Autosomal recessive spastic paraplegia type 70"
      },
      {
        "code" : "401840",
        "display" : "Autosomal recessive spastic paraplegia type 71"
      },
      {
        "code" : "401849",
        "display" : "Autosomal spastic paraplegia type 72"
      },
      {
        "code" : "401859",
        "display" : "Lipoic acid synthetase deficiency"
      },
      {
        "code" : "401862",
        "display" : "Lipoyl transferase 1 deficiency"
      },
      {
        "code" : "401866",
        "display" : "Childhood-onset spasticity with hyperglycinemia"
      },
      {
        "code" : "401869",
        "display" : "Multiple mitochondrial dysfunctions syndrome type 1"
      },
      {
        "code" : "401874",
        "display" : "Multiple mitochondrial dysfunctions syndrome type 2"
      },
      {
        "code" : "401901",
        "display" : "Huntington disease-like syndrome due to C9ORF72 expansions"
      },
      {
        "code" : "401911",
        "display" : "AXIN2-related polyposis"
      },
      {
        "code" : "401920",
        "display" : "Fibrolamellar hepatocellular carcinoma"
      },
      {
        "code" : "401923",
        "display" : "9q31.1q31.3 microdeletion syndrome"
      },
      {
        "code" : "401935",
        "display" : "14q24.1q24.3 microdeletion syndrome"
      },
      {
        "code" : "401942",
        "display" : "Familial median cleft of the upper and lower lips"
      },
      {
        "code" : "401945",
        "display" : "Moyamoya disease with early-onset achalasia"
      },
      {
        "code" : "401948",
        "display" : "Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency"
      },
      {
        "code" : "401953",
        "display" : "Episodic ataxia with slurred speech"
      },
      {
        "code" : "401959",
        "display" : "Partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome"
      },
      {
        "code" : "401964",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons"
      },
      {
        "code" : "401973",
        "display" : "MEND syndrome"
      },
      {
        "code" : "401979",
        "display" : "Autosomal recessive spondylometaphyseal dysplasia, Mégarbané type"
      },
      {
        "code" : "401986",
        "display" : "1p31p32 microdeletion syndrome"
      },
      {
        "code" : "401996",
        "display" : "Karyomegalic interstitial nephritis"
      },
      {
        "code" : "402003",
        "display" : "Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering"
      },
      {
        "code" : "402014",
        "display" : "Acute myeloid leukemia with t(6;9)(p23;q34)"
      },
      {
        "code" : "402017",
        "display" : "Acute myeloid leukemia with t(9;11)(p22;q23)"
      },
      {
        "code" : "402020",
        "display" : "Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2)"
      },
      {
        "code" : "402023",
        "display" : "Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)"
      },
      {
        "code" : "402026",
        "display" : "Acute myeloid leukemia with NPM1 somatic mutations"
      },
      {
        "code" : "402035",
        "display" : "Eosinophilic colitis"
      },
      {
        "code" : "402041",
        "display" : "Autosomal recessive distal renal tubular acidosis"
      },
      {
        "code" : "402075",
        "display" : "Familial bicuspid aortic valve"
      },
      {
        "code" : "402082",
        "display" : "Progressive myoclonic epilepsy type 5"
      },
      {
        "code" : "402364",
        "display" : "Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly"
      },
      {
        "code" : "402823",
        "display" : "Hepatitis delta"
      },
      {
        "code" : "403",
        "display" : "Familial hyperaldosteronism type I"
      },
      {
        "code" : "40366",
        "display" : "Acitretin/etretinate embryopathy"
      },
      {
        "code" : "404",
        "display" : "Familial hyperaldosteronism type II"
      },
      {
        "code" : "404437",
        "display" : "Diffuse cerebral and cerebellar atrophy-intractable seizures-progressive microcephaly syndrome"
      },
      {
        "code" : "404443",
        "display" : "Tatton-Brown-Rahman syndrome"
      },
      {
        "code" : "404448",
        "display" : "ADNP syndrome"
      },
      {
        "code" : "404451",
        "display" : "FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome"
      },
      {
        "code" : "404454",
        "display" : "Alacrimia-choreoathetosis-liver dysfunction syndrome"
      },
      {
        "code" : "404463",
        "display" : "Multisystemic smooth muscle dysfunction syndrome"
      },
      {
        "code" : "404466",
        "display" : "Female infertility due to zona pellucida defect"
      },
      {
        "code" : "404473",
        "display" : "Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome"
      },
      {
        "code" : "404476",
        "display" : "Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome"
      },
      {
        "code" : "404493",
        "display" : "Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency"
      },
      {
        "code" : "404499",
        "display" : "Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency"
      },
      {
        "code" : "404507",
        "display" : "Chondromyxoid fibroma"
      },
      {
        "code" : "404511",
        "display" : "Clear cell papillary renal cell carcinoma"
      },
      {
        "code" : "404514",
        "display" : "Acquired cystic disease-associated renal cell carcinoma"
      },
      {
        "code" : "404521",
        "display" : "Spinal muscular atrophy with respiratory distress type 2"
      },
      {
        "code" : "404546",
        "display" : "DITRA"
      },
      {
        "code" : "404553",
        "display" : "Deficiency of adenosine deaminase 2"
      },
      {
        "code" : "404560",
        "display" : "Familial atypical multiple mole melanoma syndrome"
      },
      {
        "code" : "405",
        "display" : "Familial hypocalciuric hypercalcemia"
      },
      {
        "code" : "407",
        "display" : "Glycine encephalopathy"
      },
      {
        "code" : "408",
        "display" : "Isolated glycerol kinase deficiency"
      },
      {
        "code" : "409",
        "display" : "Hyperkeratosis lenticularis perstans"
      },
      {
        "code" : "40923",
        "display" : "Eales disease"
      },
      {
        "code" : "41",
        "display" : "Dyschromatosis symmetrica hereditaria"
      },
      {
        "code" : "411493",
        "display" : "Pontocerebellar hypoplasia type 10"
      },
      {
        "code" : "411501",
        "display" : "Williams-Campbell syndrome"
      },
      {
        "code" : "411511",
        "display" : "Angelman syndrome due to a point mutation"
      },
      {
        "code" : "411515",
        "display" : "Angelman syndrome due to imprinting defect in 15q11-q13"
      },
      {
        "code" : "411527",
        "display" : "Central retinal vein occlusion"
      },
      {
        "code" : "411536",
        "display" : "Mild phosphoribosylpyrophosphate synthetase superactivity"
      },
      {
        "code" : "411543",
        "display" : "Severe phosphoribosylpyrophosphate synthetase superactivity"
      },
      {
        "code" : "411590",
        "display" : "Wolfram-like syndrome"
      },
      {
        "code" : "411593",
        "display" : "Insulin autoimmune syndrome"
      },
      {
        "code" : "411602",
        "display" : "Hereditary late-onset Parkinson disease"
      },
      {
        "code" : "411629",
        "display" : "Infantile nephropathic cystinosis"
      },
      {
        "code" : "411634",
        "display" : "Juvenile nephropathic cystinosis"
      },
      {
        "code" : "411641",
        "display" : "Ocular cystinosis"
      },
      {
        "code" : "411696",
        "display" : "Proton-pump inhibitor-responsive esophageal eosinophilia"
      },
      {
        "code" : "411703",
        "display" : "Pulmonary non-tuberculous mycobacterial infection"
      },
      {
        "code" : "411709",
        "display" : "Renal agenesis"
      },
      {
        "code" : "411712",
        "display" : "Maternal riboflavin deficiency"
      },
      {
        "code" : "411777",
        "display" : "Generalized eruptive keratoacanthoma"
      },
      {
        "code" : "411788",
        "display" : "Familial isolated trichomegaly"
      },
      {
        "code" : "411986",
        "display" : "Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome"
      },
      {
        "code" : "412",
        "display" : "Dysbetalipoproteinemia"
      },
      {
        "code" : "412022",
        "display" : "Facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome"
      },
      {
        "code" : "412035",
        "display" : "13q12.3 microdeletion syndrome"
      },
      {
        "code" : "412057",
        "display" : "Autosomal recessive cerebellar ataxia due to STUB1 deficiency"
      },
      {
        "code" : "412066",
        "display" : "PRKAR1B-related neurodegenerative dementia with intermediate filaments"
      },
      {
        "code" : "412069",
        "display" : "AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome"
      },
      {
        "code" : "412181",
        "display" : "Epidermolysis bullosa simplex due to BP230 deficiency"
      },
      {
        "code" : "412189",
        "display" : "Epidermolysis bullosa simplex due to exophilin 5 deficiency"
      },
      {
        "code" : "412206",
        "display" : "Primary failure of tooth eruption"
      },
      {
        "code" : "412217",
        "display" : "Dystonia-aphonia syndrome"
      },
      {
        "code" : "414",
        "display" : "Gyrate atrophy of choroid and retina"
      },
      {
        "code" : "415",
        "display" : "Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome"
      },
      {
        "code" : "416",
        "display" : "Primary hyperoxaluria"
      },
      {
        "code" : "417",
        "display" : "Neonatal severe primary hyperparathyroidism"
      },
      {
        "code" : "41751",
        "display" : "Bietti crystalline dystrophy"
      },
      {
        "code" : "418945",
        "display" : "Carcinoma of esophagus, salivary gland type"
      },
      {
        "code" : "418951",
        "display" : "Undifferentiated carcinoma of esophagus"
      },
      {
        "code" : "418959",
        "display" : "Squamous cell carcinoma of the stomach"
      },
      {
        "code" : "419",
        "display" : "Hyperprolinemia type 1"
      },
      {
        "code" : "42",
        "display" : "Medium chain acyl-CoA dehydrogenase deficiency"
      },
      {
        "code" : "420179",
        "display" : "Malan overgrowth syndrome"
      },
      {
        "code" : "420259",
        "display" : "Secondary pulmonary alveolar proteinosis"
      },
      {
        "code" : "420402",
        "display" : "Semicircular canal dehiscence syndrome"
      },
      {
        "code" : "420429",
        "display" : "Glycogen storage disease due to acid maltase deficiency, late-onset"
      },
      {
        "code" : "420485",
        "display" : "Cranio-cervical dystonia with laryngeal and upper-limb involvement"
      },
      {
        "code" : "420492",
        "display" : "Adult-onset cervical dystonia, DYT23 type"
      },
      {
        "code" : "420556",
        "display" : "Visual snow syndrome"
      },
      {
        "code" : "420561",
        "display" : "Temple-Baraitser syndrome"
      },
      {
        "code" : "420566",
        "display" : "Bleeding disorder due to CalDAG-GEFI deficiency"
      },
      {
        "code" : "420573",
        "display" : "Severe combined immunodeficiency due to CTPS1 deficiency"
      },
      {
        "code" : "420584",
        "display" : "Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome"
      },
      {
        "code" : "420611",
        "display" : "Transient myeloproliferative syndrome"
      },
      {
        "code" : "42062",
        "display" : "Iminoglycinuria"
      },
      {
        "code" : "420686",
        "display" : "Woolly hair-palmoplantar keratoderma syndrome"
      },
      {
        "code" : "420699",
        "display" : "Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency"
      },
      {
        "code" : "420702",
        "display" : "Autosomal recessive severe congenital neutropenia due to CSF3R deficiency"
      },
      {
        "code" : "420728",
        "display" : "Combined oxidative phosphorylation defect type 20"
      },
      {
        "code" : "420733",
        "display" : "Combined oxidative phosphorylation defect type 21"
      },
      {
        "code" : "420741",
        "display" : "RIDDLE syndrome"
      },
      {
        "code" : "420789",
        "display" : "Autoimmune encephalopathy with parasomnia and obstructive sleep apnea"
      },
      {
        "code" : "420794",
        "display" : "Cono-spondylar dysplasia"
      },
      {
        "code" : "422",
        "display" : "Idiopathic/heritable pulmonary arterial hypertension"
      },
      {
        "code" : "422526",
        "display" : "Hereditary clear cell renal cell carcinoma"
      },
      {
        "code" : "423",
        "display" : "Malignant hyperthermia of anesthesia"
      },
      {
        "code" : "423275",
        "display" : "Spinocerebellar ataxia type 40"
      },
      {
        "code" : "423296",
        "display" : "Spinocerebellar ataxia type 38"
      },
      {
        "code" : "423306",
        "display" : "Microcephaly-short stature-intellectual disability-facial dysmorphism syndrome"
      },
      {
        "code" : "423384",
        "display" : "Severe congenital neutropenia due to JAGN1 deficiency"
      },
      {
        "code" : "423454",
        "display" : "Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome"
      },
      {
        "code" : "423461",
        "display" : "Mucolipidosis type III alpha/beta"
      },
      {
        "code" : "423470",
        "display" : "Mucolipidosis type III gamma"
      },
      {
        "code" : "423479",
        "display" : "X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency"
      },
      {
        "code" : "423693",
        "display" : "Double outlet right ventricle with subaortic or doubly committed ventricular septal defect"
      },
      {
        "code" : "423712",
        "display" : "Double outlet right ventricle with atrioventricular septal defect, pulmonary stenosis, heterotaxy"
      },
      {
        "code" : "423717",
        "display" : "Cutaneous larva migrans"
      },
      {
        "code" : "423786",
        "display" : "Undifferentiated carcinoma of stomach"
      },
      {
        "code" : "423894",
        "display" : "Microcephaly-complex motor and sensory axonal neuropathy syndrome"
      },
      {
        "code" : "423968",
        "display" : "Squamous cell carcinoma of the small intestine"
      },
      {
        "code" : "423994",
        "display" : "Squamous cell carcinoma of the colon"
      },
      {
        "code" : "424",
        "display" : "Familial hyperthyroidism due to mutations in TSH receptor"
      },
      {
        "code" : "424002",
        "display" : "Squamous cell carcinoma of the rectum"
      },
      {
        "code" : "424016",
        "display" : "Adenocarcinoma of the anal canal"
      },
      {
        "code" : "424019",
        "display" : "Squamous cell carcinoma of the anal canal"
      },
      {
        "code" : "424027",
        "display" : "Progressive myoclonic epilepsy type 8"
      },
      {
        "code" : "424039",
        "display" : "Squamous cell carcinoma of pancreas"
      },
      {
        "code" : "424046",
        "display" : "Acinar cell carcinoma of pancreas"
      },
      {
        "code" : "424053",
        "display" : "Mucinous cystadenocarcinoma of the pancreas"
      },
      {
        "code" : "424058",
        "display" : "Intraductal papillary mucinous carcinoma of pancreas"
      },
      {
        "code" : "424065",
        "display" : "Pancreatic solid pseudopapillary neoplasm"
      },
      {
        "code" : "424073",
        "display" : "Serous cystadenocarcinoma of pancreas"
      },
      {
        "code" : "424080",
        "display" : "Undifferentiated carcinoma with osteoclast-like giant cells of pancreas"
      },
      {
        "code" : "424099",
        "display" : "Colobomatous microphthalmia-rhizomelic dysplasia syndrome"
      },
      {
        "code" : "424107",
        "display" : "Congenital myopathy with myasthenic-like onset"
      },
      {
        "code" : "424261",
        "display" : "TOR1AIP1-related limb-girdle muscular dystrophy"
      },
      {
        "code" : "424943",
        "display" : "Adenocarcinoma of the liver and intrahepatic biliary tract"
      },
      {
        "code" : "424970",
        "display" : "Undifferentiated carcinoma of liver and intrahepatic biliary tract"
      },
      {
        "code" : "424975",
        "display" : "Squamous cell carcinoma of liver and intrahepatic biliary tract"
      },
      {
        "code" : "424982",
        "display" : "Biliary cystadenocarcinoma"
      },
      {
        "code" : "424991",
        "display" : "Adenocarcinoma of the gallbladder and extrahepatic biliary tract"
      },
      {
        "code" : "424996",
        "display" : "Squamous cell carcinoma of gallbladder and extrahepatic biliary tract"
      },
      {
        "code" : "425",
        "display" : "Apolipoprotein A-I deficiency"
      },
      {
        "code" : "425120",
        "display" : "STING-associated vasculopathy with onset in infancy"
      },
      {
        "code" : "42642",
        "display" : "PFAPA syndrome"
      },
      {
        "code" : "42665",
        "display" : "Tietz syndrome"
      },
      {
        "code" : "427",
        "display" : "Familial hypoaldosteronism"
      },
      {
        "code" : "42775",
        "display" : "PHACE syndrome"
      },
      {
        "code" : "428",
        "display" : "Autosomal dominant hypocalcemia"
      },
      {
        "code" : "429",
        "display" : "Hypochondroplasia"
      },
      {
        "code" : "43",
        "display" : "X-linked adrenoleukodystrophy"
      },
      {
        "code" : "431140",
        "display" : "X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome"
      },
      {
        "code" : "431149",
        "display" : "Combined immunodeficiency due to OX40 deficiency"
      },
      {
        "code" : "43115",
        "display" : "Hereditary myopathy with lactic acidosis due to ISCU deficiency"
      },
      {
        "code" : "43116",
        "display" : "Serotonin syndrome"
      },
      {
        "code" : "431166",
        "display" : "Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection"
      },
      {
        "code" : "43117",
        "display" : "Acute tricyclic antidepressant poisoning"
      },
      {
        "code" : "43119",
        "display" : "Acute poisoning by drugs with membrane-stabilizing effect"
      },
      {
        "code" : "431255",
        "display" : "Scapuloperoneal spinal muscular atrophy"
      },
      {
        "code" : "431272",
        "display" : "X-linked scapuloperoneal muscular dystrophy"
      },
      {
        "code" : "431329",
        "display" : "Autosomal recessive spastic paraplegia type 57"
      },
      {
        "code" : "431341",
        "display" : "Patent urachus"
      },
      {
        "code" : "431344",
        "display" : "Urachal sinus"
      },
      {
        "code" : "431347",
        "display" : "Urachal diverticulum"
      },
      {
        "code" : "431361",
        "display" : "Progressive encephalopathy with leukodystrophy due to DECR deficiency"
      },
      {
        "code" : "432",
        "display" : "Normosmic congenital hypogonadotropic hypogonadism"
      },
      {
        "code" : "43393",
        "display" : "Lambert-Eaton myasthenic syndrome"
      },
      {
        "code" : "434179",
        "display" : "Orofaciodigital syndrome type 14"
      },
      {
        "code" : "435329",
        "display" : "Familial ossifying fibroma"
      },
      {
        "code" : "435372",
        "display" : "Anterior urethral valve"
      },
      {
        "code" : "435387",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2Y"
      },
      {
        "code" : "435438",
        "display" : "Progressive myoclonic epilepsy type 7"
      },
      {
        "code" : "435628",
        "display" : "Keppen-Lubinsky syndrome"
      },
      {
        "code" : "435638",
        "display" : "3p25.3 microdeletion syndrome"
      },
      {
        "code" : "435651",
        "display" : "CIDEC-related familial partial lipodystrophy"
      },
      {
        "code" : "435660",
        "display" : "LIPE-related familial partial lipodystrophy"
      },
      {
        "code" : "435804",
        "display" : "Short stature-advanced bone age-early-onset osteoarthritis syndrome"
      },
      {
        "code" : "435819",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation"
      },
      {
        "code" : "435845",
        "display" : "Lethal neonatal spasticity-epileptic encephalopathy syndrome"
      },
      {
        "code" : "435930",
        "display" : "Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome"
      },
      {
        "code" : "435934",
        "display" : "COG2-CDG"
      },
      {
        "code" : "435938",
        "display" : "X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome"
      },
      {
        "code" : "435953",
        "display" : "Progeroid features-hepatocellular carcinoma predisposition syndrome"
      },
      {
        "code" : "435988",
        "display" : "Chronic atrial and intestinal dysrhythmia syndrome"
      },
      {
        "code" : "435998",
        "display" : "Autosomal recessive intermediate Charcot-Marie-Tooth disease type D"
      },
      {
        "code" : "436",
        "display" : "Hypophosphatasia"
      },
      {
        "code" : "436003",
        "display" : "Contractures-developmental delay-Pierre Robin syndrome"
      },
      {
        "code" : "436141",
        "display" : "HIDEA syndrome"
      },
      {
        "code" : "436144",
        "display" : "Intrauterine growth restriction-short stature-early adult-onset diabetes syndrome"
      },
      {
        "code" : "436151",
        "display" : "Intellectual disability-expressive aphasia-facial dysmorphism syndrome"
      },
      {
        "code" : "436159",
        "display" : "Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency"
      },
      {
        "code" : "436166",
        "display" : "Periodic fever-infantile enterocolitis-autoinflammatory syndrome"
      },
      {
        "code" : "436169",
        "display" : "Thrombomodulin-related bleeding disorder"
      },
      {
        "code" : "436174",
        "display" : "Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome"
      },
      {
        "code" : "436182",
        "display" : "Microcephalic primordial dwarfism-insulin resistance syndrome"
      },
      {
        "code" : "436242",
        "display" : "Hereditary atrial tachyarrhythmia-infra-Hisian cardiac conduction disease"
      },
      {
        "code" : "436245",
        "display" : "Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome"
      },
      {
        "code" : "436252",
        "display" : "Combined immunodeficiency-multiple intestinal atresia"
      },
      {
        "code" : "436271",
        "display" : "Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy"
      },
      {
        "code" : "436274",
        "display" : "Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa"
      },
      {
        "code" : "437552",
        "display" : "Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity"
      },
      {
        "code" : "438075",
        "display" : "Ketoacidosis due to monocarboxylate transporter-1 deficiency"
      },
      {
        "code" : "438114",
        "display" : "RARS-related autosomal recessive hypomyelinating leukodystrophy"
      },
      {
        "code" : "438117",
        "display" : "Steel syndrome"
      },
      {
        "code" : "438134",
        "display" : "PCNA-related progressive neurodegenerative photosensitivity syndrome"
      },
      {
        "code" : "438159",
        "display" : "STAT3-related early-onset multisystem autoimmune disease"
      },
      {
        "code" : "438178",
        "display" : "Fatty acyl-CoA reductase 1 deficiency"
      },
      {
        "code" : "438207",
        "display" : "Severe autosomal recessive macrothrombocytopenia"
      },
      {
        "code" : "438213",
        "display" : "PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome"
      },
      {
        "code" : "438216",
        "display" : "PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation"
      },
      {
        "code" : "438266",
        "display" : "Progressive encephalomyelitis with rigidity and myoclonus"
      },
      {
        "code" : "438274",
        "display" : "GCGR-related hyperglucagonemia"
      },
      {
        "code" : "438279",
        "display" : "Human infection by orthopoxvirus"
      },
      {
        "code" : "439",
        "display" : "Isolated right ventricular hypoplasia"
      },
      {
        "code" : "439167",
        "display" : "Placental insufficiency"
      },
      {
        "code" : "439175",
        "display" : "Pediatric arterial ischemic stroke"
      },
      {
        "code" : "439196",
        "display" : "Zinc-responsive necrolytic acral erythema"
      },
      {
        "code" : "439202",
        "display" : "Non-recovering obstetric brachial plexus lesion"
      },
      {
        "code" : "439212",
        "display" : "Early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome"
      },
      {
        "code" : "439218",
        "display" : "KCNQ2-related developmental and epileptic encephalopathy"
      },
      {
        "code" : "439224",
        "display" : "ALECT2 amyloidosis"
      },
      {
        "code" : "439232",
        "display" : "AApoAIV amyloidosis"
      },
      {
        "code" : "439254",
        "display" : "ITM2B amyloidosis"
      },
      {
        "code" : "439729",
        "display" : "Cutaneous polyarteritis nodosa"
      },
      {
        "code" : "439737",
        "display" : "Primary polyarteritis nodosa"
      },
      {
        "code" : "439746",
        "display" : "Secondary polyarteritis nodosa"
      },
      {
        "code" : "439755",
        "display" : "Single-organ polyarteritis nodosa"
      },
      {
        "code" : "439762",
        "display" : "Systemic polyarteritis nodosa"
      },
      {
        "code" : "439822",
        "display" : "PDE4D haploinsufficiency syndrome"
      },
      {
        "code" : "439854",
        "display" : "Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease"
      },
      {
        "code" : "439881",
        "display" : "Plastic bronchitis"
      },
      {
        "code" : "439897",
        "display" : "Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome"
      },
      {
        "code" : "44",
        "display" : "Neonatal adrenoleukodystrophy"
      },
      {
        "code" : "440221",
        "display" : "Congenital oculomotor nerve palsy"
      },
      {
        "code" : "440233",
        "display" : "Congenital abducens nerve palsy"
      },
      {
        "code" : "440354",
        "display" : "Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome"
      },
      {
        "code" : "440368",
        "display" : "Necrotizing soft tissue infection"
      },
      {
        "code" : "440392",
        "display" : "Interstitial lung disease due to SP-C deficiency"
      },
      {
        "code" : "440402",
        "display" : "Interstitial lung disease due to ABCA3 deficiency"
      },
      {
        "code" : "440427",
        "display" : "Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency"
      },
      {
        "code" : "440437",
        "display" : "Familial colorectal cancer Type X"
      },
      {
        "code" : "440706",
        "display" : "Ribose-5-P isomerase deficiency"
      },
      {
        "code" : "440713",
        "display" : "Isolated sedoheptulokinase deficiency"
      },
      {
        "code" : "440724",
        "display" : "Extensive peripapillary myelinated nerve fibers"
      },
      {
        "code" : "440727",
        "display" : "Combined hamartoma of the retina and retinal pigment epithelium"
      },
      {
        "code" : "440731",
        "display" : "L-ferritin deficiency"
      },
      {
        "code" : "440987",
        "display" : "Isolated agenesis of gallbladder"
      },
      {
        "code" : "441",
        "display" : "Pure autonomic failure"
      },
      {
        "code" : "441447",
        "display" : "Early-onset posterior subcapsular cataract"
      },
      {
        "code" : "441452",
        "display" : "Early-onset lamellar cataract"
      },
      {
        "code" : "442582",
        "display" : "AH amyloidosis"
      },
      {
        "code" : "442835",
        "display" : "Non-specific early-onset epileptic encephalopathy"
      },
      {
        "code" : "443057",
        "display" : "Sporadic porphyria cutanea tarda"
      },
      {
        "code" : "443062",
        "display" : "Familial porphyria cutanea tarda"
      },
      {
        "code" : "443070",
        "display" : "Hemicrania continua"
      },
      {
        "code" : "443073",
        "display" : "Charcot-Marie-Tooth disease type 2S"
      },
      {
        "code" : "443079",
        "display" : "Central serous chorioretinopathy"
      },
      {
        "code" : "443084",
        "display" : "Baroreflex failure"
      },
      {
        "code" : "443087",
        "display" : "46,XY difference of sex development due to testicular 17,20-desmolase deficiency"
      },
      {
        "code" : "443098",
        "display" : "Hyperostosis cranialis interna"
      },
      {
        "code" : "443101",
        "display" : "Hypothalamic adipsic hypernatraemia syndrome"
      },
      {
        "code" : "443159",
        "display" : "Lymphoplasmacytic lymphoma without IgM production"
      },
      {
        "code" : "443162",
        "display" : "NDE1-related microhydranencephaly"
      },
      {
        "code" : "443167",
        "display" : "NUT midline carcinoma"
      },
      {
        "code" : "443173",
        "display" : "Postpartum psychosis"
      },
      {
        "code" : "443180",
        "display" : "Spontaneous intracranial hypotension"
      },
      {
        "code" : "443192",
        "display" : "Classic stiff person syndrome"
      },
      {
        "code" : "443197",
        "display" : "X-linked erythropoietic protoporphyria"
      },
      {
        "code" : "443227",
        "display" : "Paratyphoid fever"
      },
      {
        "code" : "443236",
        "display" : "Postural orthostatic tachycardia syndrome due to NET deficiency"
      },
      {
        "code" : "443291",
        "display" : "HIV-associated cancer"
      },
      {
        "code" : "443804",
        "display" : "Focal stiff limb syndrome"
      },
      {
        "code" : "443811",
        "display" : "PGM3-CDG"
      },
      {
        "code" : "443950",
        "display" : "DNAJB2-related Charcot-Marie-Tooth disease type 2"
      },
      {
        "code" : "443988",
        "display" : "Ventriculomegaly-cystic kidney disease"
      },
      {
        "code" : "443995",
        "display" : "Mandibulofacial dysostosis with alopecia"
      },
      {
        "code" : "444",
        "display" : "Marie Unna hereditary hypotrichosis"
      },
      {
        "code" : "444002",
        "display" : "11q22.2q22.3 microdeletion syndrome"
      },
      {
        "code" : "444013",
        "display" : "Combined oxidative phosphorylation defect type 23"
      },
      {
        "code" : "444048",
        "display" : "46,XX ovarian dysgenesis-short stature syndrome"
      },
      {
        "code" : "444051",
        "display" : "20q11.2 microdeletion syndrome"
      },
      {
        "code" : "444069",
        "display" : "Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome"
      },
      {
        "code" : "444072",
        "display" : "Cerebellar-facial-dental syndrome"
      },
      {
        "code" : "444077",
        "display" : "Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome"
      },
      {
        "code" : "444092",
        "display" : "Autoimmune interstitial lung disease-arthritis syndrome"
      },
      {
        "code" : "444099",
        "display" : "Autosomal dominant spastic paraplegia type 73"
      },
      {
        "code" : "444138",
        "display" : "Peeling skin-leukonychia-acral punctate keratoses-cheilitis-knuckle pads syndrome"
      },
      {
        "code" : "444316",
        "display" : "Idiopathic phalangeal acro-osteolysis"
      },
      {
        "code" : "444458",
        "display" : "Combined oxidative phosphorylation defect type 24"
      },
      {
        "code" : "444463",
        "display" : "Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency"
      },
      {
        "code" : "444490",
        "display" : "Familial chylomicronemia syndrome"
      },
      {
        "code" : "445018",
        "display" : "Combined immunodeficiency due to LRBA deficiency"
      },
      {
        "code" : "445038",
        "display" : "3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome"
      },
      {
        "code" : "445062",
        "display" : "Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome"
      },
      {
        "code" : "445110",
        "display" : "Limb-girdle muscular dystrophy due to POMK deficiency"
      },
      {
        "code" : "446",
        "display" : "Neonatal hemochromatosis"
      },
      {
        "code" : "447",
        "display" : "Paroxysmal nocturnal hemoglobinuria"
      },
      {
        "code" : "447731",
        "display" : "NIK deficiency"
      },
      {
        "code" : "447737",
        "display" : "Combined immunodeficiency due to DOCK2 deficiency"
      },
      {
        "code" : "447740",
        "display" : "Aggressive periodontitis"
      },
      {
        "code" : "447753",
        "display" : "Autosomal dominant spastic paraplegia type 9A"
      },
      {
        "code" : "447757",
        "display" : "Autosomal dominant spastic paraplegia type 9B"
      },
      {
        "code" : "447760",
        "display" : "Autosomal recessive spastic paraplegia type 9B"
      },
      {
        "code" : "447764",
        "display" : "IgG4-related sclerosing cholangitis"
      },
      {
        "code" : "447774",
        "display" : "Secondary sclerosing cholangitis"
      },
      {
        "code" : "447777",
        "display" : "Keratocystic odontogenic tumor"
      },
      {
        "code" : "447784",
        "display" : "Mitochondrial pyruvate carrier deficiency"
      },
      {
        "code" : "447788",
        "display" : "Cerebral visual impairment"
      },
      {
        "code" : "447795",
        "display" : "Lipoyl transferase 2 deficiency"
      },
      {
        "code" : "447877",
        "display" : "Polymerase proofreading-related polyposis"
      },
      {
        "code" : "447881",
        "display" : "Idiopathic dropped head syndrome"
      },
      {
        "code" : "447893",
        "display" : "Hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome"
      },
      {
        "code" : "447896",
        "display" : "Tremor-ataxia-central hypomyelination syndrome"
      },
      {
        "code" : "447954",
        "display" : "Combined oxidative phosphorylation defect type 25"
      },
      {
        "code" : "447961",
        "display" : "Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome"
      },
      {
        "code" : "447964",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2V"
      },
      {
        "code" : "447974",
        "display" : "Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome"
      },
      {
        "code" : "447977",
        "display" : "Progressive scapulohumeroperoneal distal myopathy"
      },
      {
        "code" : "447980",
        "display" : "19p13.3 microduplication syndrome"
      },
      {
        "code" : "447997",
        "display" : "Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome"
      },
      {
        "code" : "448010",
        "display" : "CAD-CDG"
      },
      {
        "code" : "448237",
        "display" : "Zika virus disease"
      },
      {
        "code" : "448242",
        "display" : "Autosomal recessive brachyolmia"
      },
      {
        "code" : "448251",
        "display" : "Progressive autosomal recessive ataxia-deafness syndrome"
      },
      {
        "code" : "448264",
        "display" : "Isolated focal non-epidermolytic palmoplantar keratoderma"
      },
      {
        "code" : "448267",
        "display" : "Regressive spondylometaphyseal dysplasia"
      },
      {
        "code" : "448270",
        "display" : "Ectopia cordis"
      },
      {
        "code" : "44890",
        "display" : "Gastrointestinal stromal tumor"
      },
      {
        "code" : "449",
        "display" : "Hepatoblastoma"
      },
      {
        "code" : "449266",
        "display" : "Pleural empyema"
      },
      {
        "code" : "449280",
        "display" : "Scedosporiosis"
      },
      {
        "code" : "449285",
        "display" : "Snakebite envenomation"
      },
      {
        "code" : "449395",
        "display" : "IgG4-related kidney disease"
      },
      {
        "code" : "449400",
        "display" : "IgG4-related aortitis"
      },
      {
        "code" : "449427",
        "display" : "IgG4-related pachymeningitis"
      },
      {
        "code" : "449432",
        "display" : "IgG4-related submandibular gland disease"
      },
      {
        "code" : "449563",
        "display" : "IgG4-related ophthalmic disease"
      },
      {
        "code" : "449566",
        "display" : "Eosinophilic angiocentric fibrosis"
      },
      {
        "code" : "45",
        "display" : "Adenosine monophosphate deaminase deficiency"
      },
      {
        "code" : "450322",
        "display" : "Polyclonal hyperviscosity syndrome"
      },
      {
        "code" : "451602",
        "display" : "Primary cutaneous plasmacytosis"
      },
      {
        "code" : "451607",
        "display" : "Cutaneous pseudolymphoma"
      },
      {
        "code" : "451612",
        "display" : "Familial congenital nasolacrimal duct obstruction"
      },
      {
        "code" : "452",
        "display" : "X-linked lissencephaly with abnormal genitalia"
      },
      {
        "code" : "453499",
        "display" : "Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome"
      },
      {
        "code" : "453504",
        "display" : "Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation"
      },
      {
        "code" : "453510",
        "display" : "Congenital insensitivity to pain with severe intellectual disability"
      },
      {
        "code" : "453521",
        "display" : "Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency"
      },
      {
        "code" : "453533",
        "display" : "Polyendocrine-polyneuropathy syndrome"
      },
      {
        "code" : "45358",
        "display" : "Congenital fibrosis of extraocular muscles"
      },
      {
        "code" : "454",
        "display" : "Acquired ichthyosis"
      },
      {
        "code" : "45448",
        "display" : "Miyoshi myopathy"
      },
      {
        "code" : "45452",
        "display" : "Idiopathic neonatal atrial flutter"
      },
      {
        "code" : "45453",
        "display" : "Incessant infant ventricular tachycardia"
      },
      {
        "code" : "454706",
        "display" : "Progressive muscular atrophy"
      },
      {
        "code" : "454710",
        "display" : "Anti-p200 pemphigoid"
      },
      {
        "code" : "454714",
        "display" : "Plasma cell leukemia"
      },
      {
        "code" : "454718",
        "display" : "Holmes-Adie syndrome"
      },
      {
        "code" : "454723",
        "display" : "Endometrioid carcinoma of ovary"
      },
      {
        "code" : "454742",
        "display" : "Variably protease-sensitive prionopathy"
      },
      {
        "code" : "454745",
        "display" : "Kuru"
      },
      {
        "code" : "454750",
        "display" : "Isolated tracheoesophageal fistula"
      },
      {
        "code" : "454831",
        "display" : "Acute radiation syndrome"
      },
      {
        "code" : "454836",
        "display" : "Avian influenza"
      },
      {
        "code" : "454840",
        "display" : "NTHL1-related polyposis"
      },
      {
        "code" : "454887",
        "display" : "Corticobasal syndrome"
      },
      {
        "code" : "455",
        "display" : "Superficial epidermolytic ichthyosis"
      },
      {
        "code" : "456298",
        "display" : "1p35.2 microdeletion syndrome"
      },
      {
        "code" : "456312",
        "display" : "Infantile multisystem neurologic-endocrine-pancreatic disease"
      },
      {
        "code" : "456318",
        "display" : "Hereditary sensory neuropathy-deafness-dementia syndrome"
      },
      {
        "code" : "456328",
        "display" : "X-linked myotubular myopathy-abnormal genitalia syndrome"
      },
      {
        "code" : "456333",
        "display" : "Hereditary neuroendocrine tumor of small intestine"
      },
      {
        "code" : "456369",
        "display" : "Polyglucosan body myopathy type 2"
      },
      {
        "code" : "457",
        "display" : "Harlequin ichthyosis"
      },
      {
        "code" : "457050",
        "display" : "Autosomal dominant mitochondrial myopathy with exercise intolerance"
      },
      {
        "code" : "457077",
        "display" : "TAFRO syndrome"
      },
      {
        "code" : "457083",
        "display" : "Isolated splenogonadal fusion"
      },
      {
        "code" : "457088",
        "display" : "Predisposition to invasive fungal disease due to CARD9 deficiency"
      },
      {
        "code" : "457095",
        "display" : "Actinomycosis"
      },
      {
        "code" : "457185",
        "display" : "Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome"
      },
      {
        "code" : "457193",
        "display" : "KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome"
      },
      {
        "code" : "457205",
        "display" : "Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome"
      },
      {
        "code" : "457212",
        "display" : "Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome"
      },
      {
        "code" : "457223",
        "display" : "Syndromic sensorineural deafness due to combined oxidative phosphorylation defect"
      },
      {
        "code" : "457240",
        "display" : "X-linked intellectual disability-short stature-overweight syndrome"
      },
      {
        "code" : "457246",
        "display" : "Clear cell sarcoma of kidney"
      },
      {
        "code" : "457260",
        "display" : "X-linked intellectual disability-hypotonia-movement disorder syndrome"
      },
      {
        "code" : "457265",
        "display" : "Progressive myoclonic epilepsy type 9"
      },
      {
        "code" : "457279",
        "display" : "Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome"
      },
      {
        "code" : "457284",
        "display" : "Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome"
      },
      {
        "code" : "457351",
        "display" : "Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome"
      },
      {
        "code" : "457359",
        "display" : "Megalencephaly-severe kyphoscoliosis-overgrowth syndrome"
      },
      {
        "code" : "457365",
        "display" : "Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome"
      },
      {
        "code" : "457375",
        "display" : "ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement"
      },
      {
        "code" : "457378",
        "display" : "Complex lethal osteochondrodysplasia"
      },
      {
        "code" : "457395",
        "display" : "Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome"
      },
      {
        "code" : "457406",
        "display" : "Multiple mitochondrial dysfunctions syndrome type 4"
      },
      {
        "code" : "457485",
        "display" : "Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome"
      },
      {
        "code" : "458718",
        "display" : "Idiopathic spontaneous coronary artery dissection"
      },
      {
        "code" : "458758",
        "display" : "Composite hemangioendothelioma"
      },
      {
        "code" : "458763",
        "display" : "Retiform hemangioendothelioma"
      },
      {
        "code" : "458768",
        "display" : "Papillary intralymphatic angioendothelioma"
      },
      {
        "code" : "458785",
        "display" : "Partially involuting congenital hemangioma"
      },
      {
        "code" : "458792",
        "display" : "Mixed cystic lymphatic malformation"
      },
      {
        "code" : "458798",
        "display" : "Spinocerebellar ataxia type 41"
      },
      {
        "code" : "458803",
        "display" : "Spinocerebellar ataxia type 42"
      },
      {
        "code" : "459033",
        "display" : "Ataxia-oculomotor apraxia type 4"
      },
      {
        "code" : "459051",
        "display" : "Spondyloepiphyseal dysplasia, Stanescu type"
      },
      {
        "code" : "459056",
        "display" : "Autosomal recessive spastic paraplegia type 75"
      },
      {
        "code" : "459061",
        "display" : "Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome"
      },
      {
        "code" : "459070",
        "display" : "X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome"
      },
      {
        "code" : "459074",
        "display" : "Corpus callosum agenesis-macrocephaly-hypertelorism syndrome"
      },
      {
        "code" : "46",
        "display" : "Adenylosuccinate lyase deficiency"
      },
      {
        "code" : "46059",
        "display" : "Lathosterolosis"
      },
      {
        "code" : "461",
        "display" : "Recessive X-linked ichthyosis"
      },
      {
        "code" : "46135",
        "display" : "Primary central nervous system lymphoma"
      },
      {
        "code" : "46348",
        "display" : "Paroxysmal extreme pain disorder"
      },
      {
        "code" : "464",
        "display" : "Incontinentia pigmenti"
      },
      {
        "code" : "464282",
        "display" : "Spastic paraplegia-severe developmental delay-epilepsy syndrome"
      },
      {
        "code" : "464288",
        "display" : "Short stature-brachydactyly-obesity-global developmental delay syndrome"
      },
      {
        "code" : "464306",
        "display" : "DYRK1A-related intellectual disability syndrome"
      },
      {
        "code" : "464311",
        "display" : "Intellectual disability syndrome due to a DYRK1A point mutation"
      },
      {
        "code" : "464318",
        "display" : "Verrucous hemangioma"
      },
      {
        "code" : "464321",
        "display" : "Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome"
      },
      {
        "code" : "464329",
        "display" : "Kaposiform lymphangiomatosis"
      },
      {
        "code" : "464336",
        "display" : "BENTA disease"
      },
      {
        "code" : "464343",
        "display" : "Catastrophic antiphospholipid syndrome"
      },
      {
        "code" : "464359",
        "display" : "Benign metanephric tumor"
      },
      {
        "code" : "464366",
        "display" : "NEK9-related lethal skeletal dysplasia"
      },
      {
        "code" : "464370",
        "display" : "Neonatal alloimmune neutropenia"
      },
      {
        "code" : "464440",
        "display" : "Primary dystonia, DYT27 type"
      },
      {
        "code" : "464443",
        "display" : "COG6-CGD"
      },
      {
        "code" : "464453",
        "display" : "Acquired methemoglobinemia"
      },
      {
        "code" : "464458",
        "display" : "Paracetamol poisoning"
      },
      {
        "code" : "464724",
        "display" : "Fever-associated acute infantile liver failure syndrome"
      },
      {
        "code" : "464738",
        "display" : "Basel-Vanagaite-Smirin-Yosef syndrome"
      },
      {
        "code" : "464756",
        "display" : "Familial gastric type 1 neuroendocrine tumor"
      },
      {
        "code" : "464760",
        "display" : "Familial cavitary optic disc anomaly"
      },
      {
        "code" : "46486",
        "display" : "Mucous membrane pemphigoid"
      },
      {
        "code" : "46487",
        "display" : "Epidermolysis bullosa acquisita"
      },
      {
        "code" : "46488",
        "display" : "Linear IgA dermatosis"
      },
      {
        "code" : "465",
        "display" : "Congenital plasminogen activator inhibitor type 1 deficiency"
      },
      {
        "code" : "46532",
        "display" : "Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome"
      },
      {
        "code" : "465508",
        "display" : "Symptomatic form of HFE-related hemochromatosis"
      },
      {
        "code" : "465824",
        "display" : "Fetal encasement syndrome"
      },
      {
        "code" : "466",
        "display" : "Fatal familial insomnia"
      },
      {
        "code" : "466026",
        "display" : "Class I glucose-6-phosphate dehydrogenase deficiency"
      },
      {
        "code" : "46627",
        "display" : "Char syndrome"
      },
      {
        "code" : "466650",
        "display" : "Exercise-induced malignant hyperthermia"
      },
      {
        "code" : "466670",
        "display" : "Cyanide poisoning"
      },
      {
        "code" : "466677",
        "display" : "Scorpion envenomation"
      },
      {
        "code" : "466682",
        "display" : "Euthyroid Graves orbitopathy"
      },
      {
        "code" : "466688",
        "display" : "Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome"
      },
      {
        "code" : "466695",
        "display" : "Supratip dysplasia"
      },
      {
        "code" : "466703",
        "display" : "TMEM199-CDG"
      },
      {
        "code" : "466718",
        "display" : "Martinique crinkled retinal pigment epitheliopathy"
      },
      {
        "code" : "466722",
        "display" : "Autosomal recessive spastic paraplegia type 77"
      },
      {
        "code" : "466729",
        "display" : "Familial patent arterial duct"
      },
      {
        "code" : "466768",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2Z"
      },
      {
        "code" : "466775",
        "display" : "Autosomal recessive Charcot-Marie-Tooth disease type 2X"
      },
      {
        "code" : "466784",
        "display" : "Neonatal severe cardiopulmonary failure due to mitochondrial methylation defect"
      },
      {
        "code" : "466791",
        "display" : "Macrocephaly-intellectual disability-left ventricular non compaction syndrome"
      },
      {
        "code" : "466794",
        "display" : "Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome"
      },
      {
        "code" : "466806",
        "display" : "Autosomal dominant thrombocytopenia with platelet secretion defect"
      },
      {
        "code" : "466921",
        "display" : "Childhood-onset progressive contractures-limb-girdle weakness-muscle dystrophy syndrome"
      },
      {
        "code" : "466926",
        "display" : "Seizures-scoliosis-macrocephaly syndrome"
      },
      {
        "code" : "466934",
        "display" : "VPS11-related autosomal recessive hypomyelinating leukodystrophy"
      },
      {
        "code" : "466943",
        "display" : "WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome"
      },
      {
        "code" : "466950",
        "display" : "Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation"
      },
      {
        "code" : "466962",
        "display" : "SMARCA4-deficient sarcoma of thorax"
      },
      {
        "code" : "467166",
        "display" : "Tubulinopathy-associated dysgyria"
      },
      {
        "code" : "467176",
        "display" : "Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome"
      },
      {
        "code" : "46724",
        "display" : "Cerebral arteriovenous malformation"
      },
      {
        "code" : "468620",
        "display" : "Intellectual disability-epilepsy-extrapyramidal syndrome"
      },
      {
        "code" : "468631",
        "display" : "Microcephalic cortical malformations-short stature due to RTTN deficiency"
      },
      {
        "code" : "468635",
        "display" : "Cryptogenic multifocal ulcerous stenosing enteritis"
      },
      {
        "code" : "468641",
        "display" : "Chronic enteropathy associated with SLCO2A1 gene"
      },
      {
        "code" : "468661",
        "display" : "Autosomal recessive spastic paraplegia type 74"
      },
      {
        "code" : "468666",
        "display" : "Isolated generalized anhidrosis with normal sweat glands"
      },
      {
        "code" : "468672",
        "display" : "Colobomatous macrophthalmia-microcornea syndrome"
      },
      {
        "code" : "468678",
        "display" : "White-Sutton syndrome"
      },
      {
        "code" : "468684",
        "display" : "CCDC115-CDG"
      },
      {
        "code" : "468699",
        "display" : "SLC39A8-CDG"
      },
      {
        "code" : "468717",
        "display" : "Rhizomelic chondrodysplasia punctata type 5"
      },
      {
        "code" : "468726",
        "display" : "Severe primary trimethylaminuria"
      },
      {
        "code" : "469",
        "display" : "Hereditary fructose intolerance"
      },
      {
        "code" : "47",
        "display" : "X-linked agammaglobulinemia"
      },
      {
        "code" : "470",
        "display" : "Lysinuric protein intolerance"
      },
      {
        "code" : "47044",
        "display" : "Hereditary papillary renal cell carcinoma"
      },
      {
        "code" : "47045",
        "display" : "Familial cold urticaria"
      },
      {
        "code" : "47159",
        "display" : "Proximal renal tubular acidosis"
      },
      {
        "code" : "472",
        "display" : "Isosporiasis"
      },
      {
        "code" : "474",
        "display" : "Jeune syndrome"
      },
      {
        "code" : "475",
        "display" : "Isolated Joubert syndrome"
      },
      {
        "code" : "476084",
        "display" : "BVES-related limb-girdle muscular dystrophy"
      },
      {
        "code" : "476093",
        "display" : "Autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome"
      },
      {
        "code" : "476096",
        "display" : "Erythrokeratodermia-cardiomyopathy syndrome"
      },
      {
        "code" : "476113",
        "display" : "Combined immunodeficiency due to TFRC deficiency"
      },
      {
        "code" : "476119",
        "display" : "Autosomal dominant preaxial polydactyly-upperback hypertrichosis syndrome"
      },
      {
        "code" : "47612",
        "display" : "Felty syndrome"
      },
      {
        "code" : "476126",
        "display" : "Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome"
      },
      {
        "code" : "476394",
        "display" : "PMP2-related Charcot-Marie-Tooth disease type 1"
      },
      {
        "code" : "476406",
        "display" : "Congenital generalized hypercontractile muscle stiffness syndrome"
      },
      {
        "code" : "477",
        "display" : "KID syndrome"
      },
      {
        "code" : "477650",
        "display" : "Fibroblastic rheumatism"
      },
      {
        "code" : "477661",
        "display" : "IL21-related infantile inflammatory bowel disease"
      },
      {
        "code" : "477673",
        "display" : "Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome"
      },
      {
        "code" : "477684",
        "display" : "Combined oxidative phosphorylation defect type 26"
      },
      {
        "code" : "477738",
        "display" : "Pediatric multiple sclerosis"
      },
      {
        "code" : "477742",
        "display" : "Nodular fasciitis"
      },
      {
        "code" : "477749",
        "display" : "Pontine autosomal dominant microangiopathy with leukoencephalopathy"
      },
      {
        "code" : "477774",
        "display" : "Combined oxidative phosphorylation defect type 27"
      },
      {
        "code" : "477781",
        "display" : "Primary condylar hyperplasia"
      },
      {
        "code" : "477787",
        "display" : "Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder"
      },
      {
        "code" : "477814",
        "display" : "Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome"
      },
      {
        "code" : "477817",
        "display" : "PMP22-RAI1 contiguous gene duplication syndrome"
      },
      {
        "code" : "477831",
        "display" : "Kosaki overgrowth syndrome"
      },
      {
        "code" : "477857",
        "display" : "Mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency"
      },
      {
        "code" : "477993",
        "display" : "Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome"
      },
      {
        "code" : "478",
        "display" : "Kallmann syndrome"
      },
      {
        "code" : "478029",
        "display" : "Combined oxidative phosphorylation defect type 29"
      },
      {
        "code" : "478042",
        "display" : "Combined oxidative phosphorylation defect type 30"
      },
      {
        "code" : "478049",
        "display" : "Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome"
      },
      {
        "code" : "478664",
        "display" : "Hereditary sensory and autonomic neuropathy type 8"
      },
      {
        "code" : "48",
        "display" : "Congenital bilateral absence of vas deferens"
      },
      {
        "code" : "480",
        "display" : "Kearns-Sayre syndrome"
      },
      {
        "code" : "480476",
        "display" : "Progressive familial intrahepatic cholestasis type 5"
      },
      {
        "code" : "480483",
        "display" : "Progressive familial intrahepatic cholestasis type 4"
      },
      {
        "code" : "480491",
        "display" : "MYO5B-related progressive familial intrahepatic cholestasis"
      },
      {
        "code" : "480501",
        "display" : "Choledochal cyst"
      },
      {
        "code" : "480506",
        "display" : "Primary intrahepatic lithiasis"
      },
      {
        "code" : "480512",
        "display" : "Idiopathic ductopenia"
      },
      {
        "code" : "480520",
        "display" : "Caroli syndrome"
      },
      {
        "code" : "480524",
        "display" : "Idiopathic peliosis hepatis"
      },
      {
        "code" : "480528",
        "display" : "Lethal hydranencephaly-diaphragmatic hernia syndrome"
      },
      {
        "code" : "480531",
        "display" : "Congenital portosystemic shunt"
      },
      {
        "code" : "480536",
        "display" : "MSH3-related polyposis"
      },
      {
        "code" : "480541",
        "display" : "High grade B-cell lymphoma with MYC and/ or BCL2 and/or BCL6 rearrangement"
      },
      {
        "code" : "480553",
        "display" : "Aneurysmal bone cyst"
      },
      {
        "code" : "480556",
        "display" : "Isolated neonatal sclerosing cholangitis"
      },
      {
        "code" : "480682",
        "display" : "POGLUT1-related limb-girdle muscular dystrophy R21"
      },
      {
        "code" : "480701",
        "display" : "Facial diplegia with paresthesias"
      },
      {
        "code" : "480851",
        "display" : "Hereditary thrombocytopenia with early-onset myelofibrosis"
      },
      {
        "code" : "480864",
        "display" : "Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome"
      },
      {
        "code" : "480880",
        "display" : "X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability"
      },
      {
        "code" : "480898",
        "display" : "Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome"
      },
      {
        "code" : "480907",
        "display" : "X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome"
      },
      {
        "code" : "481",
        "display" : "Kennedy disease"
      },
      {
        "code" : "48104",
        "display" : "Pyoderma gangrenosum"
      },
      {
        "code" : "481152",
        "display" : "PYCR2-related microcephaly-progressive leukoencephalopathy"
      },
      {
        "code" : "48162",
        "display" : "Lewis-Sumner syndrome"
      },
      {
        "code" : "481662",
        "display" : "Familial Chilblain lupus"
      },
      {
        "code" : "481665",
        "display" : "USP18 deficiency"
      },
      {
        "code" : "481986",
        "display" : "Familial schizencephaly"
      },
      {
        "code" : "482",
        "display" : "Kimura disease"
      },
      {
        "code" : "482077",
        "display" : "HTRA1-related autosomal dominant cerebral small vessel disease"
      },
      {
        "code" : "482601",
        "display" : "Adenylosuccinate synthetase-like 1-related distal myopathy"
      },
      {
        "code" : "482606",
        "display" : "X-linked keloid scarring-reduced joint mobility-increased optic cup-to-disc ratio syndrome"
      },
      {
        "code" : "483",
        "display" : "Congenital high-molecular-weight kininogen deficiency"
      },
      {
        "code" : "48372",
        "display" : "Nodular regenerative hyperplasia of the liver"
      },
      {
        "code" : "48377",
        "display" : "Subcorneal pustular dermatosis"
      },
      {
        "code" : "48431",
        "display" : "Congenital cataracts-facial dysmorphism-neuropathy syndrome"
      },
      {
        "code" : "48435",
        "display" : "Postinfectious vasculitis"
      },
      {
        "code" : "485",
        "display" : "Kniest dysplasia"
      },
      {
        "code" : "485275",
        "display" : "Acquired schizencephaly"
      },
      {
        "code" : "485350",
        "display" : "CLCN4-related X-linked intellectual disability syndrome"
      },
      {
        "code" : "485358",
        "display" : "Propylthiouracil embryofetopathy"
      },
      {
        "code" : "485405",
        "display" : "16p12.1p12.3 triplication syndrome"
      },
      {
        "code" : "485418",
        "display" : "EMILIN-1-related connective tissue disease"
      },
      {
        "code" : "485421",
        "display" : "MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect"
      },
      {
        "code" : "485426",
        "display" : "Isolated congenital hepatic fibrosis"
      },
      {
        "code" : "486",
        "display" : "Autosomal dominant severe congenital neutropenia"
      },
      {
        "code" : "48652",
        "display" : "Phelan-McDermid syndrome"
      },
      {
        "code" : "486811",
        "display" : "Prenatal-onset spinal muscular atrophy with congenital bone fractures"
      },
      {
        "code" : "486815",
        "display" : "Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome"
      },
      {
        "code" : "48686",
        "display" : "Primary effusion lymphoma"
      },
      {
        "code" : "487",
        "display" : "Krabbe disease"
      },
      {
        "code" : "48736",
        "display" : "Embryonal carcinoma of the central nervous system"
      },
      {
        "code" : "487796",
        "display" : "Takenouchi-Kosaki syndrome"
      },
      {
        "code" : "487809",
        "display" : "Pediatric collagenous gastritis"
      },
      {
        "code" : "487814",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation"
      },
      {
        "code" : "487825",
        "display" : "Pierpont syndrome"
      },
      {
        "code" : "488",
        "display" : "Urachal cyst"
      },
      {
        "code" : "488168",
        "display" : "Microcephaly-congenital cataract-psoriasiform dermatitis syndrome"
      },
      {
        "code" : "48818",
        "display" : "Aceruloplasminemia"
      },
      {
        "code" : "488191",
        "display" : "Female infertility due to oocyte meiotic arrest"
      },
      {
        "code" : "488197",
        "display" : "Familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome"
      },
      {
        "code" : "488232",
        "display" : "Split-foot malformation-mesoaxial polydactyly syndrome"
      },
      {
        "code" : "488239",
        "display" : "Acute macular neuroretinopathy"
      },
      {
        "code" : "488265",
        "display" : "Osteofibrous dysplasia"
      },
      {
        "code" : "488280",
        "display" : "14q32 duplication syndrome"
      },
      {
        "code" : "488333",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2W"
      },
      {
        "code" : "488434",
        "display" : "Camptodactyly syndrome, Guadalajara type 3"
      },
      {
        "code" : "488437",
        "display" : "SIX2-related frontonasal dysplasia"
      },
      {
        "code" : "488586",
        "display" : "Congenital amyoplasia"
      },
      {
        "code" : "488594",
        "display" : "Autosomal recessive spastic paraplegia type 76"
      },
      {
        "code" : "488613",
        "display" : "Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome"
      },
      {
        "code" : "488618",
        "display" : "Transketolase deficiency"
      },
      {
        "code" : "488627",
        "display" : "Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome"
      },
      {
        "code" : "488632",
        "display" : "TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome"
      },
      {
        "code" : "488635",
        "display" : "Early-onset epilepsy-intellectual disability-brain anomalies syndrome"
      },
      {
        "code" : "488642",
        "display" : "TELO2-related intellectual disability-neurodevelopmental disorder"
      },
      {
        "code" : "488647",
        "display" : "DDX41-related hematologic malignancy predisposition syndrome"
      },
      {
        "code" : "488650",
        "display" : "Distal myopathy, Tateyama type"
      },
      {
        "code" : "48918",
        "display" : "Focal myositis"
      },
      {
        "code" : "49",
        "display" : "Penile agenesis"
      },
      {
        "code" : "490",
        "display" : "Omphalomesenteric cyst"
      },
      {
        "code" : "49041",
        "display" : "IgG4-related retroperitoneal fibrosis"
      },
      {
        "code" : "49042",
        "display" : "Dentinogenesis imperfecta"
      },
      {
        "code" : "492",
        "display" : "Proliferating trichilemmal cyst"
      },
      {
        "code" : "493",
        "display" : "Familial keratoacanthoma"
      },
      {
        "code" : "493342",
        "display" : "Vibratory urticaria"
      },
      {
        "code" : "49382",
        "display" : "Achromatopsia"
      },
      {
        "code" : "494",
        "display" : "Keratoderma hereditarium mutilans"
      },
      {
        "code" : "494344",
        "display" : "RERE-related neurodevelopmental syndrome"
      },
      {
        "code" : "494418",
        "display" : "Vulvar carcinoma"
      },
      {
        "code" : "494421",
        "display" : "Sacrococcygeal teratoma"
      },
      {
        "code" : "494424",
        "display" : "Extracranial carotid artery aneurysm"
      },
      {
        "code" : "494428",
        "display" : "Idiopathic pleuroparenchymal fibroelastosis"
      },
      {
        "code" : "494433",
        "display" : "MIRAGE syndrome"
      },
      {
        "code" : "494439",
        "display" : "Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome"
      },
      {
        "code" : "494444",
        "display" : "DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome"
      },
      {
        "code" : "494448",
        "display" : "Vulvar squamous cell carcinoma"
      },
      {
        "code" : "494451",
        "display" : "Vulvar basal cell carcinoma"
      },
      {
        "code" : "494454",
        "display" : "Vulvar adenocarcinoma"
      },
      {
        "code" : "494526",
        "display" : "Infantile-onset generalized dyskinesia with orofacial involvement"
      },
      {
        "code" : "494541",
        "display" : "Childhood-onset benign chorea with striatal involvement"
      },
      {
        "code" : "494547",
        "display" : "Squamous cell carcinoma of the hypopharynx"
      },
      {
        "code" : "494550",
        "display" : "Squamous cell carcinoma of the larynx"
      },
      {
        "code" : "495",
        "display" : "Transgrediens et progrediens palmoplantar keratoderma"
      },
      {
        "code" : "495274",
        "display" : "Charcot-Marie-Tooth disease type 2T"
      },
      {
        "code" : "49566",
        "display" : "Acquired purpura fulminans"
      },
      {
        "code" : "495818",
        "display" : "9q33.3q34.11 microdeletion syndrome"
      },
      {
        "code" : "495844",
        "display" : "C11ORF73-related autosomal recessive hypomyelinating leukodystrophy"
      },
      {
        "code" : "495875",
        "display" : "Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome"
      },
      {
        "code" : "495879",
        "display" : "Congenital agenesis of the scrotum"
      },
      {
        "code" : "495930",
        "display" : "Familial monosomy 7 syndrome"
      },
      {
        "code" : "496641",
        "display" : "Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome"
      },
      {
        "code" : "496686",
        "display" : "Kyphosis-lateral tongue atrophy-myofibrillar myopathy syndrome"
      },
      {
        "code" : "496689",
        "display" : "Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome"
      },
      {
        "code" : "496693",
        "display" : "Omphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome"
      },
      {
        "code" : "496751",
        "display" : "EVEN-plus syndrome"
      },
      {
        "code" : "496756",
        "display" : "Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome"
      },
      {
        "code" : "496790",
        "display" : "Ocular anomalies-axonal neuropathy-developmental delay syndrome"
      },
      {
        "code" : "497188",
        "display" : "Diffuse intrinsic pontine glioma"
      },
      {
        "code" : "497737",
        "display" : "Epidermolytic nevus"
      },
      {
        "code" : "497757",
        "display" : "MME-related autosomal dominant Charcot Marie Tooth disease type 2"
      },
      {
        "code" : "497764",
        "display" : "Spinocerebellar ataxia type 43"
      },
      {
        "code" : "497906",
        "display" : "Childhood-onset basal ganglia degeneration syndrome"
      },
      {
        "code" : "49804",
        "display" : "Lichen amyloidosis"
      },
      {
        "code" : "498228",
        "display" : "Phyllodes tumor of the prostate"
      },
      {
        "code" : "498251",
        "display" : "Menstrual cycle-dependent periodic fever"
      },
      {
        "code" : "49827",
        "display" : "Thiamine-responsive megaloblastic anemia syndrome"
      },
      {
        "code" : "498359",
        "display" : "Aquagenic palmoplantar keratoderma"
      },
      {
        "code" : "498474",
        "display" : "Hyaline fibromatosis syndrome"
      },
      {
        "code" : "498481",
        "display" : "LRP5-related primary osteoporosis"
      },
      {
        "code" : "498485",
        "display" : "Overgrowth-metaphyseal undermodeling-spondylar dysplasia syndrome"
      },
      {
        "code" : "498488",
        "display" : "Overgrowth syndrome with 2q37 translocation"
      },
      {
        "code" : "498494",
        "display" : "Mirror-image polydactyly"
      },
      {
        "code" : "498497",
        "display" : "Short rib-polydactyly syndrome type 5"
      },
      {
        "code" : "498602",
        "display" : "Sugarman brachydactyly"
      },
      {
        "code" : "498693",
        "display" : "MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome"
      },
      {
        "code" : "499",
        "display" : "Kerion celsi"
      },
      {
        "code" : "499009",
        "display" : "Congenital syphilis"
      },
      {
        "code" : "499085",
        "display" : "Chronic relapsing inflammatory optic neuritis"
      },
      {
        "code" : "499096",
        "display" : "Isolated optic neuritis"
      },
      {
        "code" : "499103",
        "display" : "Recurrent idiopathic neuroretinitis"
      },
      {
        "code" : "499107",
        "display" : "Idiopathic optic perineuritis"
      },
      {
        "code" : "499182",
        "display" : "Pilomatrix carcinoma"
      },
      {
        "code" : "5",
        "display" : "Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency"
      },
      {
        "code" : "50",
        "display" : "Aicardi syndrome"
      },
      {
        "code" : "500",
        "display" : "Noonan syndrome with multiple lentigines"
      },
      {
        "code" : "500055",
        "display" : "Hao-Fountain syndrome due to 16p13.2 microdeletion"
      },
      {
        "code" : "500062",
        "display" : "Infantile-onset periodic fever-panniculitis-dermatosis syndrome"
      },
      {
        "code" : "500095",
        "display" : "Tall stature-intellectual disability-renal anomalies syndrome"
      },
      {
        "code" : "500135",
        "display" : "Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome"
      },
      {
        "code" : "500144",
        "display" : "Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome"
      },
      {
        "code" : "500150",
        "display" : "Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome"
      },
      {
        "code" : "500159",
        "display" : "Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom"
      },
      {
        "code" : "500163",
        "display" : "Witteveen-Kolk syndrome"
      },
      {
        "code" : "500166",
        "display" : "SIN3-related intellectual disability syndrome due to a point mutation"
      },
      {
        "code" : "500180",
        "display" : "Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder"
      },
      {
        "code" : "500188",
        "display" : "X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome"
      },
      {
        "code" : "500464",
        "display" : "Squamous cell carcinoma of the nasal cavity and paranasal sinuses"
      },
      {
        "code" : "500478",
        "display" : "Squamous cell carcinoma of the oropharynx"
      },
      {
        "code" : "500533",
        "display" : "Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome"
      },
      {
        "code" : "500545",
        "display" : "Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract"
      },
      {
        "code" : "500548",
        "display" : "Osteosclerotic metaphyseal dysplasia"
      },
      {
        "code" : "501",
        "display" : "Lafora disease"
      },
      {
        "code" : "502",
        "display" : "Trichorhinophalangeal syndrome type 2"
      },
      {
        "code" : "502305",
        "display" : "Cochleovestibular malformation"
      },
      {
        "code" : "502318",
        "display" : "Cochlear nerve deficiency"
      },
      {
        "code" : "502363",
        "display" : "Squamous cell carcinoma of the oral cavity"
      },
      {
        "code" : "502366",
        "display" : "Squamous cell carcinoma of the lip"
      },
      {
        "code" : "502423",
        "display" : "Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome"
      },
      {
        "code" : "502430",
        "display" : "Weiss-Kruszka Syndrome"
      },
      {
        "code" : "502434",
        "display" : "STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome"
      },
      {
        "code" : "502437",
        "display" : "4q25 proximal deletion syndrome"
      },
      {
        "code" : "502444",
        "display" : "Alkaline ceramidase 3 deficiency"
      },
      {
        "code" : "502499",
        "display" : "Erythema multiforme major"
      },
      {
        "code" : "50251",
        "display" : "Pleural mesothelioma"
      },
      {
        "code" : "503",
        "display" : "Larsen syndrome"
      },
      {
        "code" : "504",
        "display" : "Creeping myiasis"
      },
      {
        "code" : "504476",
        "display" : "Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome"
      },
      {
        "code" : "504523",
        "display" : "Severe combined immunodeficiency due to LAT deficiency"
      },
      {
        "code" : "504530",
        "display" : "Combined immunodeficiency due to Moesin deficiency"
      },
      {
        "code" : "505",
        "display" : "Graham Little-Piccardi-Lassueur syndrome"
      },
      {
        "code" : "505208",
        "display" : "3-methylglutaconic aciduria type 8"
      },
      {
        "code" : "505216",
        "display" : "3-methylglutaconic aciduria type 9"
      },
      {
        "code" : "505227",
        "display" : "Combined immunodeficiency due to GINS1 deficiency"
      },
      {
        "code" : "505237",
        "display" : "Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome"
      },
      {
        "code" : "505242",
        "display" : "Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome"
      },
      {
        "code" : "505248",
        "display" : "Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders"
      },
      {
        "code" : "505395",
        "display" : "Ventilator-induced diaphragmatic dysfunction"
      },
      {
        "code" : "505652",
        "display" : "CDKL5-deficiency disorder"
      },
      {
        "code" : "506",
        "display" : "Leigh syndrome"
      },
      {
        "code" : "506075",
        "display" : "Non-functioning neuroendocrine tumor of pancreas"
      },
      {
        "code" : "506090",
        "display" : "Serotonin-producing neuroendocrine tumor of pancreas"
      },
      {
        "code" : "506098",
        "display" : "Neuroendocrine carcinoma of pancreas"
      },
      {
        "code" : "506112",
        "display" : "Mixed neuroendocrine and non-neuroendocrine neoplasm of pancreas"
      },
      {
        "code" : "506136",
        "display" : "Neuroendocrine neoplasm of esophagus"
      },
      {
        "code" : "506307",
        "display" : "Stromme syndrome"
      },
      {
        "code" : "506334",
        "display" : "Familial steroid-resistant nephrotic syndrome with adrenal insufficiency"
      },
      {
        "code" : "506353",
        "display" : "Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction"
      },
      {
        "code" : "506358",
        "display" : "Gabriele-de Vries syndrome"
      },
      {
        "code" : "506784",
        "display" : "Stevens-Johnson syndrome/toxic epidermal necrolysis overlap syndrome"
      },
      {
        "code" : "507",
        "display" : "Leishmaniasis"
      },
      {
        "code" : "508",
        "display" : "Donohue syndrome"
      },
      {
        "code" : "50809",
        "display" : "Talo-patello-scaphoid osteolysis"
      },
      {
        "code" : "508093",
        "display" : "MEPAN syndrome"
      },
      {
        "code" : "50810",
        "display" : "Microlissencephaly-micromelia syndrome"
      },
      {
        "code" : "50811",
        "display" : "Lipodystrophy-intellectual disability-deafness syndrome"
      },
      {
        "code" : "50812",
        "display" : "Zellweger-like syndrome without peroxisomal anomalies"
      },
      {
        "code" : "50814",
        "display" : "Craniolenticulosutural dysplasia"
      },
      {
        "code" : "50815",
        "display" : "Branchiogenic deafness syndrome"
      },
      {
        "code" : "50839",
        "display" : "Cat-scratch disease"
      },
      {
        "code" : "508410",
        "display" : "Familial intestinal malrotation"
      },
      {
        "code" : "508476",
        "display" : "Cleft lip and palate-craniofacial dysmorphism-congenital heart defect-hearing loss syndrome"
      },
      {
        "code" : "508488",
        "display" : "8q24.3 microdeletion syndrome"
      },
      {
        "code" : "508498",
        "display" : "Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome"
      },
      {
        "code" : "508501",
        "display" : "Oral-facial-digital syndrome with short stature and brachymesophalangy"
      },
      {
        "code" : "508512",
        "display" : "Intrauterine growth restriction-congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome"
      },
      {
        "code" : "508523",
        "display" : "Hyperphenylalaninemia due to DNAJC12 deficiency"
      },
      {
        "code" : "508529",
        "display" : "Intermediate epidermolysis bullosa simplex with cardiomyopathy"
      },
      {
        "code" : "508533",
        "display" : "Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome"
      },
      {
        "code" : "508542",
        "display" : "Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome"
      },
      {
        "code" : "509",
        "display" : "Leptospirosis"
      },
      {
        "code" : "50918",
        "display" : "Kikuchi-Fujimoto disease"
      },
      {
        "code" : "50942",
        "display" : "Striate palmoplantar keratoderma"
      },
      {
        "code" : "50943",
        "display" : "Keratolytic winter erythema"
      },
      {
        "code" : "50944",
        "display" : "Schöpf-Schulz-Passarge syndrome"
      },
      {
        "code" : "50945",
        "display" : "Blomstrand lethal chondrodysplasia"
      },
      {
        "code" : "51",
        "display" : "Aicardi-Goutières syndrome"
      },
      {
        "code" : "510",
        "display" : "Lesch-Nyhan syndrome"
      },
      {
        "code" : "51083",
        "display" : "Congenital short QT syndrome"
      },
      {
        "code" : "51084",
        "display" : "Torsade-de-pointes syndrome with short coupling interval"
      },
      {
        "code" : "511",
        "display" : "Maple syrup urine disease"
      },
      {
        "code" : "51188",
        "display" : "Ethylmalonic encephalopathy"
      },
      {
        "code" : "512",
        "display" : "Metachromatic leukodystrophy"
      },
      {
        "code" : "512017",
        "display" : "Chronic lymphoproliferative disorder of natural killer cells"
      },
      {
        "code" : "51208",
        "display" : "Formiminoglutamic aciduria"
      },
      {
        "code" : "512103",
        "display" : "Autosomal recessive epidermolytic ichthyosis"
      },
      {
        "code" : "512260",
        "display" : "Congenital cerebellar ataxia due to RNU12 mutation"
      },
      {
        "code" : "513436",
        "display" : "Autosomal recessive spastic paraplegia type 78"
      },
      {
        "code" : "513456",
        "display" : "Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome"
      },
      {
        "code" : "514",
        "display" : "Acute monoblastic/monocytic leukemia"
      },
      {
        "code" : "514352",
        "display" : "Congenital brachyesophagus-intrathoracic stomach-vertebral anomalies syndrome"
      },
      {
        "code" : "51608",
        "display" : "Generalized arterial calcification of infancy"
      },
      {
        "code" : "51636",
        "display" : "WHIM syndrome"
      },
      {
        "code" : "517",
        "display" : "Acute myelomonocytic leukemia"
      },
      {
        "code" : "518",
        "display" : "Acute megakaryoblastic leukemia"
      },
      {
        "code" : "51890",
        "display" : "Anterior cutaneous nerve entrapment syndrome"
      },
      {
        "code" : "519384",
        "display" : "Congenital cystic eye"
      },
      {
        "code" : "519386",
        "display" : "Isolated congenital entropion"
      },
      {
        "code" : "519388",
        "display" : "Autosomal recessive anterior segment dysgenesis"
      },
      {
        "code" : "519390",
        "display" : "Isolated blepharochalasis"
      },
      {
        "code" : "519392",
        "display" : "Isolated iridoschisis"
      },
      {
        "code" : "519396",
        "display" : "Isolated microspherophakia"
      },
      {
        "code" : "519398",
        "display" : "Isolated foveal hypoplasia"
      },
      {
        "code" : "519400",
        "display" : "Peripapillary staphyloma"
      },
      {
        "code" : "519402",
        "display" : "Isolated megalopapilla"
      },
      {
        "code" : "519404",
        "display" : "Optic disc pit"
      },
      {
        "code" : "519406",
        "display" : "Thygeson superficial punctate keratitis"
      },
      {
        "code" : "519408",
        "display" : "Mooren ulcer"
      },
      {
        "code" : "519410",
        "display" : "Terrien marginal degeneration"
      },
      {
        "code" : "519930",
        "display" : "Fungal keratitis"
      },
      {
        "code" : "52",
        "display" : "Alagille syndrome"
      },
      {
        "code" : "520",
        "display" : "Acute promyelocytic leukemia"
      },
      {
        "code" : "52022",
        "display" : "Potocki-Shaffer syndrome"
      },
      {
        "code" : "52047",
        "display" : "Braddock syndrome"
      },
      {
        "code" : "52054",
        "display" : "Craniosynostosis-intracranial calcifications syndrome"
      },
      {
        "code" : "52055",
        "display" : "Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome"
      },
      {
        "code" : "52056",
        "display" : "Ulnar/fibula ray defect-brachydactyly syndrome"
      },
      {
        "code" : "521",
        "display" : "Chronic myeloid leukemia"
      },
      {
        "code" : "521123",
        "display" : "Radiation-induced plexopathy"
      },
      {
        "code" : "521127",
        "display" : "Osteoradionecrosis of the mandible"
      },
      {
        "code" : "521219",
        "display" : "Mirizzi syndrome"
      },
      {
        "code" : "521258",
        "display" : "Xq25 microduplication syndrome"
      },
      {
        "code" : "521268",
        "display" : "Sodium-dependent multivitamin transporter deficiency"
      },
      {
        "code" : "521305",
        "display" : "Proximal myopathy with focal depletion of mitochondria"
      },
      {
        "code" : "521308",
        "display" : "Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome"
      },
      {
        "code" : "521390",
        "display" : "Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome"
      },
      {
        "code" : "521406",
        "display" : "Dystonia-parkinsonism-hypermanganesemia syndrome"
      },
      {
        "code" : "521411",
        "display" : "Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect"
      },
      {
        "code" : "521414",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2DD"
      },
      {
        "code" : "521426",
        "display" : "PLAA-associated neurodevelopmental disorder"
      },
      {
        "code" : "521432",
        "display" : "Congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome"
      },
      {
        "code" : "521438",
        "display" : "Congenital vertebral-cardiac-renal anomalies syndrome"
      },
      {
        "code" : "521445",
        "display" : "Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome"
      },
      {
        "code" : "521450",
        "display" : "LAMA5-related multisystemic syndrome"
      },
      {
        "code" : "522037",
        "display" : "Primary autoimmune enteropathy"
      },
      {
        "code" : "522077",
        "display" : "Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome"
      },
      {
        "code" : "523",
        "display" : "Hereditary leiomyomatosis and renal cell cancer"
      },
      {
        "code" : "52368",
        "display" : "Mohr-Tranebjaerg syndrome"
      },
      {
        "code" : "524",
        "display" : "Li-Fraumeni syndrome"
      },
      {
        "code" : "52416",
        "display" : "Mantle cell lymphoma"
      },
      {
        "code" : "52417",
        "display" : "MALT lymphoma"
      },
      {
        "code" : "52427",
        "display" : "Retinitis punctata albescens"
      },
      {
        "code" : "52429",
        "display" : "Branchiootic syndrome"
      },
      {
        "code" : "52430",
        "display" : "Inclusion body myopathy with Paget disease of bone and frontotemporal dementia"
      },
      {
        "code" : "525",
        "display" : "Lichen planopilaris"
      },
      {
        "code" : "52503",
        "display" : "X-linked creatine transporter deficiency"
      },
      {
        "code" : "52530",
        "display" : "Pseudo-von Willebrand disease"
      },
      {
        "code" : "525731",
        "display" : "Pediatric-onset Graves disease"
      },
      {
        "code" : "525738",
        "display" : "Prepubertal anorexia nervosa"
      },
      {
        "code" : "526",
        "display" : "Liddle syndrome"
      },
      {
        "code" : "527276",
        "display" : "Encephalopathy due to mitochondrial and peroxisomal fission defect"
      },
      {
        "code" : "527450",
        "display" : "Severe myopia-generalized joint laxity-short stature syndrome"
      },
      {
        "code" : "527468",
        "display" : "Diaphragmatic hernia-short bowel-asplenia syndrome"
      },
      {
        "code" : "527497",
        "display" : "NKX6-2-related autosomal recessive hypomyelinating leukodystrophy"
      },
      {
        "code" : "528",
        "display" : "Congenital generalized lipodystrophy"
      },
      {
        "code" : "528084",
        "display" : "Non-specific syndromic intellectual disability"
      },
      {
        "code" : "528091",
        "display" : "Hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome"
      },
      {
        "code" : "528105",
        "display" : "Hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome"
      },
      {
        "code" : "528623",
        "display" : "Hereditary angioedema with C1Inh deficiency"
      },
      {
        "code" : "528647",
        "display" : "Hereditary angioedema with normal C1Inh"
      },
      {
        "code" : "528663",
        "display" : "Acquired angioedema with C1Inh deficiency"
      },
      {
        "code" : "529",
        "display" : "Roch-Leri mesosomatous lipomatosis"
      },
      {
        "code" : "52901",
        "display" : "Isolated follicle stimulating hormone deficiency"
      },
      {
        "code" : "529468",
        "display" : "Monoclonal mast cell activation syndrome"
      },
      {
        "code" : "529574",
        "display" : "Duane retraction syndrome with congenital deafness"
      },
      {
        "code" : "529665",
        "display" : "Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome"
      },
      {
        "code" : "529799",
        "display" : "Acute bilirubin encephalopathy"
      },
      {
        "code" : "529808",
        "display" : "Chronic bilirubin encephalopathy"
      },
      {
        "code" : "529831",
        "display" : "Letrozole toxicity"
      },
      {
        "code" : "529852",
        "display" : "Combined hepatocellular carcinoma and cholangiocarcinoma"
      },
      {
        "code" : "529864",
        "display" : "Secondary erythromelalgia"
      },
      {
        "code" : "52994",
        "display" : "Orbital leiomyoma"
      },
      {
        "code" : "529962",
        "display" : "17q24.2 microdeletion syndrome"
      },
      {
        "code" : "529965",
        "display" : "Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome"
      },
      {
        "code" : "529970",
        "display" : "Male infertility due to acephalic spermatozoa"
      },
      {
        "code" : "529977",
        "display" : "Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome"
      },
      {
        "code" : "529980",
        "display" : "Inflammatory bowel disease-recurrent sinopulmonary infections syndrome"
      },
      {
        "code" : "53",
        "display" : "Albers-Schönberg osteopetrosis"
      },
      {
        "code" : "530",
        "display" : "Lipoid proteinosis"
      },
      {
        "code" : "530033",
        "display" : "Dermoid or epidermoid cyst of the central nervous system"
      },
      {
        "code" : "530298",
        "display" : "Progressive myoclonic epilepsy with neuroserpin inclusion bodies"
      },
      {
        "code" : "530303",
        "display" : "Progressive dementia with neuroserpin inclusion bodies"
      },
      {
        "code" : "53035",
        "display" : "Caroli disease"
      },
      {
        "code" : "530792",
        "display" : "RELA fusion-positive ependymoma"
      },
      {
        "code" : "530838",
        "display" : "KRT1-related diffuse nonepidermolytic keratoderma"
      },
      {
        "code" : "530849",
        "display" : "Familial apolipoprotein A5 deficiency"
      },
      {
        "code" : "530983",
        "display" : "Lamb-Shaffer syndrome"
      },
      {
        "code" : "530995",
        "display" : "Mixed phenotype acute leukemia"
      },
      {
        "code" : "531",
        "display" : "Miller-Dieker syndrome"
      },
      {
        "code" : "531151",
        "display" : "9q21.13 microdeletion syndrome"
      },
      {
        "code" : "53271",
        "display" : "Muenke syndrome"
      },
      {
        "code" : "53296",
        "display" : "Familial cutaneous collagenoma"
      },
      {
        "code" : "533",
        "display" : "Listeriosis"
      },
      {
        "code" : "53347",
        "display" : "Brody myopathy"
      },
      {
        "code" : "53351",
        "display" : "X-linked dystonia-parkinsonism"
      },
      {
        "code" : "53372",
        "display" : "Hereditary geniospasm"
      },
      {
        "code" : "534",
        "display" : "Oculocerebrorenal syndrome of Lowe"
      },
      {
        "code" : "53540",
        "display" : "Goldmann-Favre syndrome"
      },
      {
        "code" : "535453",
        "display" : "Familial lipase maturation factor 1 deficiency"
      },
      {
        "code" : "535458",
        "display" : "Familial GPIHBP1 deficiency"
      },
      {
        "code" : "53583",
        "display" : "Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity"
      },
      {
        "code" : "536",
        "display" : "Systemic lupus erythematosus"
      },
      {
        "code" : "536467",
        "display" : "B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome"
      },
      {
        "code" : "536471",
        "display" : "Spondylodysplastic Ehlers-Danlos syndrome"
      },
      {
        "code" : "536516",
        "display" : "Myopathic Ehlers-Danlos syndrome"
      },
      {
        "code" : "536532",
        "display" : "Classical-like Ehlers-Danlos syndrome type 2"
      },
      {
        "code" : "536545",
        "display" : "Kyphoscoliotic Ehlers-Danlos syndrome"
      },
      {
        "code" : "53689",
        "display" : "Congenital chloride diarrhea"
      },
      {
        "code" : "53690",
        "display" : "Congenital lactase deficiency"
      },
      {
        "code" : "53691",
        "display" : "Congenital cornea plana"
      },
      {
        "code" : "53693",
        "display" : "GRACILE syndrome"
      },
      {
        "code" : "53696",
        "display" : "Arthrogryposis-anterior horn cell disease syndrome"
      },
      {
        "code" : "53697",
        "display" : "Gnathodiaphyseal dysplasia"
      },
      {
        "code" : "53698",
        "display" : "Myosin storage myopathy"
      },
      {
        "code" : "537",
        "display" : "Toxic epidermal necrolysis"
      },
      {
        "code" : "537072",
        "display" : "PLG-related hereditary angioedema with normal C1Inh"
      },
      {
        "code" : "53715",
        "display" : "Familial tumoral calcinosis"
      },
      {
        "code" : "53719",
        "display" : "Cerebrofacial arteriovenous metameric syndrome type 2"
      },
      {
        "code" : "53721",
        "display" : "Spinal arteriovenous metameric syndrome"
      },
      {
        "code" : "538",
        "display" : "Lymphangioleiomyomatosis"
      },
      {
        "code" : "538096",
        "display" : "Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy"
      },
      {
        "code" : "538101",
        "display" : "Congenital axonal neuropathy with encephalopathy"
      },
      {
        "code" : "538574",
        "display" : "Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome"
      },
      {
        "code" : "538756",
        "display" : "Familial multiple discoid fibromas"
      },
      {
        "code" : "538863",
        "display" : "Classic pyoderma gangrenosum"
      },
      {
        "code" : "538866",
        "display" : "Pustular pyoderma gangrenosum"
      },
      {
        "code" : "538869",
        "display" : "Bullous pyoderma gangrenosum"
      },
      {
        "code" : "538872",
        "display" : "Vegetative pyoderma gangrenosum"
      },
      {
        "code" : "538931",
        "display" : "X-linked lymphoproliferative disease due to SAP deficiency"
      },
      {
        "code" : "538934",
        "display" : "X-linked lymphoproliferative disease due to XIAP deficiency"
      },
      {
        "code" : "538958",
        "display" : "Combined immunodeficiency due to CD70 deficiency"
      },
      {
        "code" : "538963",
        "display" : "Combined immunodeficiency due to ITK deficiency"
      },
      {
        "code" : "54",
        "display" : "X-linked recessive ocular albinism"
      },
      {
        "code" : "540",
        "display" : "Familial hemophagocytic lymphohistiocytosis"
      },
      {
        "code" : "54028",
        "display" : "Plummer-Vinson syndrome"
      },
      {
        "code" : "54057",
        "display" : "Thrombotic thrombocytopenic purpura"
      },
      {
        "code" : "541423",
        "display" : "Growth delay-intellectual disability-hepatopathy syndrome"
      },
      {
        "code" : "541443",
        "display" : "Anomalous aortic origin of the left coronary artery"
      },
      {
        "code" : "541454",
        "display" : "Anomalous aortic origin of the right coronary artery"
      },
      {
        "code" : "541507",
        "display" : "Anomalous origin of coronary artery from the pulmonary artery"
      },
      {
        "code" : "542301",
        "display" : "Combined immunodeficiency due to CARMIL2 deficiency"
      },
      {
        "code" : "542306",
        "display" : "GNB5-related intellectual disability-cardiac arrhythmia syndrome"
      },
      {
        "code" : "542310",
        "display" : "Leukoencephalopathy with calcifications and cysts"
      },
      {
        "code" : "542323",
        "display" : "CAR T cell therapy-associated cytokine release syndrome"
      },
      {
        "code" : "54247",
        "display" : "Posterior cortical atrophy"
      },
      {
        "code" : "54251",
        "display" : "Aseptic abscess syndrome"
      },
      {
        "code" : "542568",
        "display" : "Quadricuspid aortic valve"
      },
      {
        "code" : "542585",
        "display" : "Auditory neuropathy-optic atrophy syndrome"
      },
      {
        "code" : "542592",
        "display" : "Necrobiosis lipoidica"
      },
      {
        "code" : "54260",
        "display" : "Left ventricular noncompaction"
      },
      {
        "code" : "542643",
        "display" : "Livedoid vasculopathy"
      },
      {
        "code" : "542657",
        "display" : "Isolated hyperchlorhidrosis"
      },
      {
        "code" : "54272",
        "display" : "Hepatocellular adenoma"
      },
      {
        "code" : "543",
        "display" : "Burkitt lymphoma"
      },
      {
        "code" : "543470",
        "display" : "Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome"
      },
      {
        "code" : "54368",
        "display" : "Sarcocystosis"
      },
      {
        "code" : "54370",
        "display" : "Primary membranoproliferative glomerulonephritis"
      },
      {
        "code" : "544254",
        "display" : "SYNGAP1-related developmental and epileptic encephalopathy"
      },
      {
        "code" : "544469",
        "display" : "PRUNE1-related neurological syndrome"
      },
      {
        "code" : "544472",
        "display" : "Atypical hemolytic uremic syndrome with complement gene abnormality"
      },
      {
        "code" : "544482",
        "display" : "Infection-related hemolytic uremic syndrome"
      },
      {
        "code" : "544488",
        "display" : "Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome"
      },
      {
        "code" : "544493",
        "display" : "Streptococcus pneumoniae-associated hemolytic uremic syndrome"
      },
      {
        "code" : "544503",
        "display" : "RNF13-related severe early-onset epileptic encephalopathy"
      },
      {
        "code" : "544578",
        "display" : "Congenital primary megaureter, refluxing and obstructed form"
      },
      {
        "code" : "544602",
        "display" : "Congenital myopathy with reduced type 2 muscle fibers"
      },
      {
        "code" : "544628",
        "display" : "Atypical Fanconi syndrome-neonatal hyperinsulinism syndrome"
      },
      {
        "code" : "545",
        "display" : "Follicular lymphoma"
      },
      {
        "code" : "54595",
        "display" : "Craniopharyngioma"
      },
      {
        "code" : "548",
        "display" : "Leprosy"
      },
      {
        "code" : "549",
        "display" : "Legionnaires disease"
      },
      {
        "code" : "550",
        "display" : "MELAS"
      },
      {
        "code" : "551",
        "display" : "MERRF"
      },
      {
        "code" : "552",
        "display" : "MODY"
      },
      {
        "code" : "555402",
        "display" : "NAD(P)HX dehydratase deficiency"
      },
      {
        "code" : "555407",
        "display" : "NAD(P)HX epimerase deficiency"
      },
      {
        "code" : "555434",
        "display" : "Fibrohistiocytic inflammatory pseudotumor of the liver"
      },
      {
        "code" : "555437",
        "display" : "Lymphoplasmacytic inflammatory pseudotumor of the liver"
      },
      {
        "code" : "555874",
        "display" : "Congenital tricuspid valve dysplasia"
      },
      {
        "code" : "555877",
        "display" : "FLNA-related X-linked myxomatous valvular dysplasia"
      },
      {
        "code" : "555905",
        "display" : "IgA pemphigus"
      },
      {
        "code" : "55595",
        "display" : "TNP03-related limb-girdle muscular dystrophy D2"
      },
      {
        "code" : "55596",
        "display" : "HNRNPDL-related limb-girdle muscular dystrophy D3"
      },
      {
        "code" : "556",
        "display" : "Malakoplakia"
      },
      {
        "code" : "556030",
        "display" : "Early-onset familial hypoaldosteronism"
      },
      {
        "code" : "556037",
        "display" : "Late-onset familial hypoaldosteronism"
      },
      {
        "code" : "55654",
        "display" : "Hypotrichosis simplex"
      },
      {
        "code" : "55655",
        "display" : "Pneumococcal meningitis"
      },
      {
        "code" : "556955",
        "display" : "Pancreatic agenesis-holoprosencephaly syndrome"
      },
      {
        "code" : "556985",
        "display" : "Early-onset calcifying leukoencephalopathy-skeletal dysplasia"
      },
      {
        "code" : "557003",
        "display" : "Oculoskeletodental syndrome"
      },
      {
        "code" : "557056",
        "display" : "Spastic ataxia-dysarthria due to glutaminase deficiency"
      },
      {
        "code" : "557064",
        "display" : "Neonatal epileptic encephalopathy due to glutaminase deficiency"
      },
      {
        "code" : "558",
        "display" : "Marfan syndrome"
      },
      {
        "code" : "558411",
        "display" : "Idiopathic gastroparesis"
      },
      {
        "code" : "55880",
        "display" : "Chondrosarcoma"
      },
      {
        "code" : "55881",
        "display" : "Adamantinoma"
      },
      {
        "code" : "559",
        "display" : "Marinesco-Sjögren syndrome"
      },
      {
        "code" : "56",
        "display" : "Alkaptonuria"
      },
      {
        "code" : "560",
        "display" : "Marshall syndrome"
      },
      {
        "code" : "561",
        "display" : "Marshall-Smith syndrome"
      },
      {
        "code" : "561854",
        "display" : "FOXG1 syndrome"
      },
      {
        "code" : "562",
        "display" : "McCune-Albright syndrome"
      },
      {
        "code" : "562509",
        "display" : "Heme oxygenase-1 deficiency"
      },
      {
        "code" : "562528",
        "display" : "Congenital limbs-face contractures-hypotonia-developmental delay syndrome"
      },
      {
        "code" : "562538",
        "display" : "Autosomal recessive extra-oral halitosis"
      },
      {
        "code" : "562559",
        "display" : "Anterior maxillary protrusion-strabismus-intellectual disability syndrome"
      },
      {
        "code" : "562569",
        "display" : "TMEM94-associated congenital heart defect-facial dysmorphism-developmental delay syndrome"
      },
      {
        "code" : "562639",
        "display" : "Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome"
      },
      {
        "code" : "563",
        "display" : "Peripartum cardiomyopathy"
      },
      {
        "code" : "56304",
        "display" : "Atelosteogenesis type II"
      },
      {
        "code" : "56305",
        "display" : "Atelosteogenesis type III"
      },
      {
        "code" : "563576",
        "display" : "Autoimmune hepatitis type 1"
      },
      {
        "code" : "563581",
        "display" : "Autoimmune hepatitis type 2"
      },
      {
        "code" : "563589",
        "display" : "Seronegative autoimmune hepatitis"
      },
      {
        "code" : "563609",
        "display" : "Isolated anencephaly"
      },
      {
        "code" : "563612",
        "display" : "Isolated exencephaly"
      },
      {
        "code" : "563666",
        "display" : "Serous cystadenoma of childhood"
      },
      {
        "code" : "563671",
        "display" : "Mucinous cystadenoma of childhood"
      },
      {
        "code" : "563676",
        "display" : "Seromucinous cystadenoma of childhood"
      },
      {
        "code" : "563684",
        "display" : "Furuncular myiasis due to Dermatobia hominis"
      },
      {
        "code" : "563687",
        "display" : "Furuncular myiasis due to Cordylobia anthropophaga"
      },
      {
        "code" : "563690",
        "display" : "Furuncular myiasis due to Cordylobia rodhaini"
      },
      {
        "code" : "563708",
        "display" : "Syndromic congenital sodium diarrhea"
      },
      {
        "code" : "563951",
        "display" : "Isolated congenital aglossia"
      },
      {
        "code" : "563954",
        "display" : "Isolated congenital hypoglossia"
      },
      {
        "code" : "563991",
        "display" : "Osteochondrosis of the tarsal bone"
      },
      {
        "code" : "564",
        "display" : "Meckel syndrome"
      },
      {
        "code" : "564003",
        "display" : "Osteochondrosis of the metatarsal bone"
      },
      {
        "code" : "564178",
        "display" : "Primary hypomagnesemia-refractory seizures-intellectual disability syndrome"
      },
      {
        "code" : "56425",
        "display" : "Cold agglutinin disease"
      },
      {
        "code" : "565",
        "display" : "Menkes disease"
      },
      {
        "code" : "565612",
        "display" : "Primary triglyceride deposit cardiomyovasculopathy"
      },
      {
        "code" : "565624",
        "display" : "Combined oxidative phosphorylation defect type 39"
      },
      {
        "code" : "565641",
        "display" : "Primary desmosis coli"
      },
      {
        "code" : "565782",
        "display" : "Methotrexate toxicity"
      },
      {
        "code" : "565788",
        "display" : "Infantile inflammatory bowel disease with neurological involvement"
      },
      {
        "code" : "565837",
        "display" : "Laminin subunit alpha 2-related limb-girdle muscular dystrophy R23"
      },
      {
        "code" : "565858",
        "display" : "Craniosynostosis-microretrognathia-severe intellectual disability syndrome"
      },
      {
        "code" : "565899",
        "display" : "POMGNT2-related limb-girdle muscular dystrophy R24"
      },
      {
        "code" : "565909",
        "display" : "Calpain-3-related limb-girdle muscular dystrophy D4"
      },
      {
        "code" : "566",
        "display" : "Congenital microcoria"
      },
      {
        "code" : "566067",
        "display" : "CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome"
      },
      {
        "code" : "566175",
        "display" : "Complement hyperactivation-angiopathic thrombosis-protein-losing enteropathy syndrome"
      },
      {
        "code" : "566192",
        "display" : "Congenital autosomal recessive small-platelet thrombocytopenia"
      },
      {
        "code" : "566231",
        "display" : "Resistance to thyroid hormone due to a mutation in thyroid hormone receptor alpha"
      },
      {
        "code" : "566243",
        "display" : "Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta"
      },
      {
        "code" : "566393",
        "display" : "Acute mast cell leukemia"
      },
      {
        "code" : "566396",
        "display" : "Chronic mast cell leukemia"
      },
      {
        "code" : "566841",
        "display" : "Liver adenomatosis"
      },
      {
        "code" : "566847",
        "display" : "Aprosencephaly/atelencephaly spectrum"
      },
      {
        "code" : "566852",
        "display" : "Atelencephaly"
      },
      {
        "code" : "566857",
        "display" : "Aprosencephaly"
      },
      {
        "code" : "566862",
        "display" : "Left sided atrial isomerism"
      },
      {
        "code" : "566943",
        "display" : "Mueller-Weiss syndrome"
      },
      {
        "code" : "567",
        "display" : "22q11.2 deletion syndrome"
      },
      {
        "code" : "567502",
        "display" : "B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome"
      },
      {
        "code" : "567544",
        "display" : "Idiopathic non-lupus full-house nephropathy"
      },
      {
        "code" : "567546",
        "display" : "Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance"
      },
      {
        "code" : "567548",
        "display" : "Idiopathic steroid-resistant nephrotic syndrome"
      },
      {
        "code" : "567550",
        "display" : "Idiopathic multidrug-resistant nephrotic syndrome"
      },
      {
        "code" : "567552",
        "display" : "Idiopathic steroid-resistant nephrotic syndrome with sensitivity to second-line immunosuppressive therapy"
      },
      {
        "code" : "567983",
        "display" : "Parenteral nutrition-associated cholestasis"
      },
      {
        "code" : "568",
        "display" : "Microphthalmia, Lenz type"
      },
      {
        "code" : "568051",
        "display" : "GJC2-related late-onset primary lymphedema"
      },
      {
        "code" : "568056",
        "display" : "Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome"
      },
      {
        "code" : "568062",
        "display" : "PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis"
      },
      {
        "code" : "568065",
        "display" : "EPHB4-related lymphatic-related hydrops fetalis"
      },
      {
        "code" : "569",
        "display" : "Familial or sporadic hemiplegic migraine"
      },
      {
        "code" : "569164",
        "display" : "Angiomatoid fibrous histiocytoma"
      },
      {
        "code" : "569248",
        "display" : "Microcystic stromal tumor"
      },
      {
        "code" : "569274",
        "display" : "Multiple mitochondrial dysfunctions syndrome type 5"
      },
      {
        "code" : "569290",
        "display" : "Multiple mitochondrial dysfunctions syndrome type 6"
      },
      {
        "code" : "569816",
        "display" : "CELSR1-related late-onset primary lymphedema"
      },
      {
        "code" : "569821",
        "display" : "Congenital primary lymphedema of Gordon"
      },
      {
        "code" : "57",
        "display" : "Glycogen storage disease due to aldolase A deficiency"
      },
      {
        "code" : "570",
        "display" : "Moebius syndrome"
      },
      {
        "code" : "570371",
        "display" : "Bartter syndrome type 5"
      },
      {
        "code" : "570422",
        "display" : "Galactose mutarotase deficiency"
      },
      {
        "code" : "570431",
        "display" : "Idiopathic multicentric Castleman disease"
      },
      {
        "code" : "570438",
        "display" : "HHV-8-associated multicentric Castleman disease"
      },
      {
        "code" : "570470",
        "display" : "Ricin poisoning"
      },
      {
        "code" : "570491",
        "display" : "QRSL1-related combined oxidative phosphorylation defect"
      },
      {
        "code" : "570762",
        "display" : "Infective endocarditis"
      },
      {
        "code" : "57145",
        "display" : "SUNCT syndrome"
      },
      {
        "code" : "57196",
        "display" : "Medial condensing osteitis of the clavicle"
      },
      {
        "code" : "572",
        "display" : "Immunodeficiency by defective expression of MHC class II"
      },
      {
        "code" : "572013",
        "display" : "Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome"
      },
      {
        "code" : "572333",
        "display" : "Blepharophimosis-ptosis-epicanthus inversus syndrome plus"
      },
      {
        "code" : "572354",
        "display" : "Blepharophimosis-ptosis-epicanthus inversus syndrome type 1"
      },
      {
        "code" : "572361",
        "display" : "Blepharophimosis-ptosis-epicanthus inversus syndrome type 2"
      },
      {
        "code" : "572385",
        "display" : "Brachydactyly type B1"
      },
      {
        "code" : "572428",
        "display" : "Infantile-onset pulmonary alveolar proteinosis-hypogammaglobulinemia"
      },
      {
        "code" : "572543",
        "display" : "RFVT2-related riboflavin transporter deficiency"
      },
      {
        "code" : "572550",
        "display" : "RFVT3-related riboflavin transporter deficiency"
      },
      {
        "code" : "572761",
        "display" : "DONSON-related microcephaly-short stature-limb abnormalities spectrum"
      },
      {
        "code" : "572768",
        "display" : "Microcephaly-micromelia syndrome"
      },
      {
        "code" : "572773",
        "display" : "Microcephaly-short stature-limb abnormalities syndrome"
      },
      {
        "code" : "572798",
        "display" : "WARS2-related combined oxidative phosphorylation defect"
      },
      {
        "code" : "573",
        "display" : "Monilethrix"
      },
      {
        "code" : "573253",
        "display" : "Split cord malformation type II"
      },
      {
        "code" : "574",
        "display" : "21q deletion syndrome"
      },
      {
        "code" : "574918",
        "display" : "Predisposition to severe viral infection due to IRF7 deficiency"
      },
      {
        "code" : "574957",
        "display" : "Mendelian susceptibility to mycobacterial diseases due to partial JAK1 deficiency"
      },
      {
        "code" : "575",
        "display" : "Muckle-Wells syndrome"
      },
      {
        "code" : "575553",
        "display" : "Cathepsin A-related arteriopathy-strokes-leukoencephalopathy"
      },
      {
        "code" : "576",
        "display" : "Mucolipidosis type II"
      },
      {
        "code" : "576074",
        "display" : "Middle East respiratory syndrome"
      },
      {
        "code" : "576227",
        "display" : "Complete atrioventricular septal defect without ventricular hypoplasia"
      },
      {
        "code" : "576232",
        "display" : "Partial atrioventricular septal defect with ventricular hypoplasia"
      },
      {
        "code" : "576235",
        "display" : "Partial atrioventricular septal defect without ventricular hypoplasia"
      },
      {
        "code" : "576242",
        "display" : "Intermediate atrioventricular septal defect"
      },
      {
        "code" : "576278",
        "display" : "SATB2-associated syndrome"
      },
      {
        "code" : "576283",
        "display" : "SATB2-associated syndrome due to a pathogenic variant"
      },
      {
        "code" : "576349",
        "display" : "NLRC4-related familial cold autoinflammatory syndrome"
      },
      {
        "code" : "576370",
        "display" : "Variant Creutzfeldt-Jakob disease"
      },
      {
        "code" : "576379",
        "display" : "Iatrogenic Creutzfeldt-Jakob disease"
      },
      {
        "code" : "577",
        "display" : "Mucolipidosis type III"
      },
      {
        "code" : "57782",
        "display" : "Mazabraud syndrome"
      },
      {
        "code" : "578",
        "display" : "Mucolipidosis type IV"
      },
      {
        "code" : "579",
        "display" : "Mucopolysaccharidosis type 1"
      },
      {
        "code" : "58",
        "display" : "Alexander disease"
      },
      {
        "code" : "580",
        "display" : "Mucopolysaccharidosis type 2"
      },
      {
        "code" : "58017",
        "display" : "Classic hairy cell leukemia"
      },
      {
        "code" : "58040",
        "display" : "Osteoblastoma"
      },
      {
        "code" : "580572",
        "display" : "Intraductal tubulopapillary neoplasm of pancreas"
      },
      {
        "code" : "580933",
        "display" : "Lethal brain and heart developmental defects"
      },
      {
        "code" : "580940",
        "display" : "QRICH1-related intellectual disability-chondrodysplasia syndrome"
      },
      {
        "code" : "580951",
        "display" : "Punctate inner choroidopathy"
      },
      {
        "code" : "581",
        "display" : "Mucopolysaccharidosis type 3"
      },
      {
        "code" : "581271",
        "display" : "Cramp-fasciculation syndrome"
      },
      {
        "code" : "582",
        "display" : "Mucopolysaccharidosis type 4"
      },
      {
        "code" : "583",
        "display" : "Mucopolysaccharidosis type 6"
      },
      {
        "code" : "583097",
        "display" : "Congenital infiltrating lipomatosis of the face"
      },
      {
        "code" : "583595",
        "display" : "Serine biosynthesis pathway deficiency, infantile/juvenile form"
      },
      {
        "code" : "583602",
        "display" : "Neu-Laxova syndrome due to phosphoserine aminotransferase deficiency"
      },
      {
        "code" : "583607",
        "display" : "Neu-Laxova syndrome due to 3-phosphoglycerate dehydrogenase deficiency"
      },
      {
        "code" : "583612",
        "display" : "Neu-Laxova syndrome due to 3-phosphoserine phosphatase deficiency"
      },
      {
        "code" : "583856",
        "display" : "Isolated splenic vein thrombosis"
      },
      {
        "code" : "583861",
        "display" : "Isolated mesenteric vein thrombosis"
      },
      {
        "code" : "584",
        "display" : "Mucopolysaccharidosis type 7"
      },
      {
        "code" : "585",
        "display" : "Multiple sulfatase deficiency"
      },
      {
        "code" : "585867",
        "display" : "Acute myeloid leukemia with t(9;22)(q34.1;q11.2)"
      },
      {
        "code" : "585877",
        "display" : "B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality"
      },
      {
        "code" : "585909",
        "display" : "B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)"
      },
      {
        "code" : "585918",
        "display" : "B-lymphoblastic leukemia/lymphoma with t(v;11q23.3)"
      },
      {
        "code" : "585929",
        "display" : "B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1)"
      },
      {
        "code" : "585936",
        "display" : "B-lymphoblastic leukemia/lymphoma with hyperdiploidy"
      },
      {
        "code" : "585942",
        "display" : "B-lymphoblastic leukemia/lymphoma with hypodiploidy"
      },
      {
        "code" : "585948",
        "display" : "B-lymphoblastic leukemia/lymphoma with t(5;14)(q31.1;q32.3)"
      },
      {
        "code" : "585956",
        "display" : "B-lymphoblastic leukemia/lymphoma with t(1;19)(q23;p13.3)"
      },
      {
        "code" : "586",
        "display" : "Cystic fibrosis"
      },
      {
        "code" : "586130",
        "display" : "Sporadic fatal insomnia"
      },
      {
        "code" : "588",
        "display" : "Muscle-eye-brain disease"
      },
      {
        "code" : "589",
        "display" : "Myasthenia gravis"
      },
      {
        "code" : "589435",
        "display" : "Spondylometaphyseal dysplasia-corneal dystrophy syndrome"
      },
      {
        "code" : "589442",
        "display" : "Short stature-skeletal dysplasia-retinal degeneration-intellectual disability-sensorineural hearing loss syndrome"
      },
      {
        "code" : "589515",
        "display" : "PUM1-associated developmental disability-ataxia-seizure syndrome"
      },
      {
        "code" : "589522",
        "display" : "Spinocerebellar ataxia type 46"
      },
      {
        "code" : "589527",
        "display" : "Spinocerebellar ataxia type 45"
      },
      {
        "code" : "589534",
        "display" : "Mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)"
      },
      {
        "code" : "589542",
        "display" : "Myeloid/lymphoid neoplasm associated with JAK2 rearrangement"
      },
      {
        "code" : "589547",
        "display" : "GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder"
      },
      {
        "code" : "589595",
        "display" : "Mixed phenotype acute leukemia with t(v;11q23.3)"
      },
      {
        "code" : "589608",
        "display" : "Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies"
      },
      {
        "code" : "589618",
        "display" : "Dystonia 28"
      },
      {
        "code" : "589821",
        "display" : "Congenital-onset Steinert myotonic dystrophy"
      },
      {
        "code" : "589824",
        "display" : "Childhood-onset Steinert myotonic dystrophy"
      },
      {
        "code" : "589827",
        "display" : "Juvenile-onset Steinert myotonic dystrophy"
      },
      {
        "code" : "589830",
        "display" : "Adult-onset Steinert myotonic dystrophy"
      },
      {
        "code" : "589833",
        "display" : "Late-onset Steinert myotonic dystrophy"
      },
      {
        "code" : "589856",
        "display" : "Choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome"
      },
      {
        "code" : "589905",
        "display" : "PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome"
      },
      {
        "code" : "59",
        "display" : "Allan-Herndon-Dudley syndrome"
      },
      {
        "code" : "590",
        "display" : "Congenital myasthenic syndrome"
      },
      {
        "code" : "590539",
        "display" : "Isolated melanotic schwannoma"
      },
      {
        "code" : "591",
        "display" : "Furuncular myiasis"
      },
      {
        "code" : "59135",
        "display" : "Laing distal myopathy"
      },
      {
        "code" : "59181",
        "display" : "Sorsby pseudoinflammatory fundus dystrophy"
      },
      {
        "code" : "592",
        "display" : "Macrophagic myofasciitis"
      },
      {
        "code" : "592564",
        "display" : "GNAO1-related developmental delay-seizures-movement disorder spectrum"
      },
      {
        "code" : "592570",
        "display" : "TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome"
      },
      {
        "code" : "592574",
        "display" : "Menke-Hennekam syndrome"
      },
      {
        "code" : "592850",
        "display" : "Neuromyelitis optica spectrum disorder with anti-AQP4 antibodies"
      },
      {
        "code" : "592856",
        "display" : "Neuromyelitis optica spectrum disorder with anti-MOG antibodies"
      },
      {
        "code" : "592869",
        "display" : "Neuromyelitis optica spectrum disorder without anti-MOG and without anti-AQP4 antibodies"
      },
      {
        "code" : "592873",
        "display" : "Acute transverse myelitis with anti-MOG antibodies"
      },
      {
        "code" : "592894",
        "display" : "Acute disseminated encephalomyelitis with anti-MOG antibodies"
      },
      {
        "code" : "592900",
        "display" : "Acute disseminated encephalomyelitis without anti-MOG antibodies"
      },
      {
        "code" : "59298",
        "display" : "Schilder disease"
      },
      {
        "code" : "59303",
        "display" : "Neonatal ichthyosis-sclerosing cholangitis syndrome"
      },
      {
        "code" : "59306",
        "display" : "McLeod neuroacanthocytosis syndrome"
      },
      {
        "code" : "59315",
        "display" : "Rhombencephalosynapsis"
      },
      {
        "code" : "595098",
        "display" : "Timothy syndrome type 1"
      },
      {
        "code" : "595105",
        "display" : "Timothy syndrome type 2"
      },
      {
        "code" : "595109",
        "display" : "Atypical Timothy syndrome"
      },
      {
        "code" : "595133",
        "display" : "Perivascular epithelioid cell neoplasm"
      },
      {
        "code" : "595356",
        "display" : "Localized dystrophic epidermolysis bullosa"
      },
      {
        "code" : "596",
        "display" : "X-linked centronuclear myopathy"
      },
      {
        "code" : "596008",
        "display" : "Antley-Bixler syndrome without genital anomaly or disorder of steroidogenesis"
      },
      {
        "code" : "596448",
        "display" : "IgG4-related systemic disease"
      },
      {
        "code" : "596753",
        "display" : "VEXAS syndrome"
      },
      {
        "code" : "596759",
        "display" : "Combined immunodeficiency due to RELA haploinsufficiency"
      },
      {
        "code" : "596937",
        "display" : "Portosinusoidal vascular disease"
      },
      {
        "code" : "596941",
        "display" : "Incomplete septal cirrhosis"
      },
      {
        "code" : "597",
        "display" : "Central core disease"
      },
      {
        "code" : "597201",
        "display" : "TRIM22-related inflammatory bowel disease"
      },
      {
        "code" : "597623",
        "display" : "IRF2BPL-related regressive neurodevelopmental disorder-dystonia-seizures syndrome"
      },
      {
        "code" : "597733",
        "display" : "Oculocutaneous albinism type 8"
      },
      {
        "code" : "597738",
        "display" : "Luscan-Lumish syndrome"
      },
      {
        "code" : "597743",
        "display" : "SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome"
      },
      {
        "code" : "597746",
        "display" : "Blepharophimosis-intellectual disability syndrome/genitopatellar overlap syndrome"
      },
      {
        "code" : "597874",
        "display" : "MTHFS-related developmental delay-microcephaly-short stature-epilepsy syndrome"
      },
      {
        "code" : "597887",
        "display" : "ALPI-related inflammatory bowel disease"
      },
      {
        "code" : "597939",
        "display" : "Euthyroid dysprealbuminemic hyperthyroxinemia"
      },
      {
        "code" : "598",
        "display" : "Multiminicore myopathy"
      },
      {
        "code" : "598164",
        "display" : "FOXG1 syndrome due to intragenic alteration"
      },
      {
        "code" : "598216",
        "display" : "Upper tract urothelial carcinoma"
      },
      {
        "code" : "598363",
        "display" : "Multisystem inflammatory syndrome in children and adults"
      },
      {
        "code" : "598603",
        "display" : "Facial dysmorphism-hypertrichosis-epilepsy-intellectual disability/developmental delay-gingival overgrowth syndrome"
      },
      {
        "code" : "599082",
        "display" : "CHD3-related developmental delay-speech delay-intellectual disability-abnormalities of vision-facial dysmorphism syndrome"
      },
      {
        "code" : "599373",
        "display" : "STXBP1-related encephalopathy"
      },
      {
        "code" : "599376",
        "display" : "Hypomyelination of early myelinating structures"
      },
      {
        "code" : "599418",
        "display" : "Hereditary angioedema with normal C1Inh not related to F12 or PLG variant"
      },
      {
        "code" : "599480",
        "display" : "Acquired hemophilia A"
      },
      {
        "code" : "599485",
        "display" : "Acquired hemophilia B"
      },
      {
        "code" : "599490",
        "display" : "Acquired factor V deficiency"
      },
      {
        "code" : "599495",
        "display" : "Acquired factor VII deficiency"
      },
      {
        "code" : "599501",
        "display" : "Acquired factor X deficiency"
      },
      {
        "code" : "599507",
        "display" : "Acquired factor XI deficiency"
      },
      {
        "code" : "599513",
        "display" : "Acquired factor XIII deficiency"
      },
      {
        "code" : "599519",
        "display" : "Factor V short isoforms-related bleeding disorder"
      },
      {
        "code" : "599579",
        "display" : "Factor V Amsterdam bleeding disorder"
      },
      {
        "code" : "6",
        "display" : "3-methylcrotonyl-CoA carboxylase deficiency"
      },
      {
        "code" : "60",
        "display" : "Alpha-1-antitrypsin deficiency"
      },
      {
        "code" : "600",
        "display" : "Vocal cord and pharyngeal distal myopathy"
      },
      {
        "code" : "60014",
        "display" : "Argyria"
      },
      {
        "code" : "60015",
        "display" : "Enlarged parietal foramina"
      },
      {
        "code" : "600194",
        "display" : "Factor V Atlanta bleeding disorder"
      },
      {
        "code" : "60025",
        "display" : "Pulmonary alveolar microlithiasis"
      },
      {
        "code" : "60026",
        "display" : "Pulmonary nodular lymphoid hyperplasia"
      },
      {
        "code" : "60030",
        "display" : "Loeys-Dietz syndrome"
      },
      {
        "code" : "60032",
        "display" : "Recurrent respiratory papillomatosis"
      },
      {
        "code" : "60033",
        "display" : "Idiopathic bronchiectasis"
      },
      {
        "code" : "60039",
        "display" : "Pudendal nerve entrapment syndrome"
      },
      {
        "code" : "60040",
        "display" : "Megalencephaly-capillary malformation-polymicrogyria syndrome"
      },
      {
        "code" : "60041",
        "display" : "Congenital heart block"
      },
      {
        "code" : "600663",
        "display" : "NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance"
      },
      {
        "code" : "600668",
        "display" : "CCNK-related neurodevelopmental disorder-severe intellectual disability-facial dysmorphism syndrome"
      },
      {
        "code" : "600691",
        "display" : "Combined deficiency of factor VII and factor X"
      },
      {
        "code" : "600731",
        "display" : "Clark-Baraitser syndrome"
      },
      {
        "code" : "600952",
        "display" : "Non-syndromic perineal fistula"
      },
      {
        "code" : "600961",
        "display" : "Non-syndromic rectourethral fistula"
      },
      {
        "code" : "600966",
        "display" : "Non-syndromic rectourethral fistula, bulbar type"
      },
      {
        "code" : "600975",
        "display" : "Non-syndromic rectourethral fistula, prostatic type"
      },
      {
        "code" : "600984",
        "display" : "Non-syndromic rectovesical fistula"
      },
      {
        "code" : "600993",
        "display" : "Non-syndromic vestibular fistula"
      },
      {
        "code" : "600998",
        "display" : "Non-syndromic cloacal malformation"
      },
      {
        "code" : "601002",
        "display" : "Non-syndromic anorectal malformation without fistula"
      },
      {
        "code" : "601008",
        "display" : "Non-syndromic anal stenosis"
      },
      {
        "code" : "601013",
        "display" : "Non-syndromic pouch colon"
      },
      {
        "code" : "601018",
        "display" : "Non-syndromic rectal atresia"
      },
      {
        "code" : "601023",
        "display" : "Non-syndromic rectal stenosis"
      },
      {
        "code" : "601028",
        "display" : "Non-syndromic rectovaginal fistula"
      },
      {
        "code" : "601033",
        "display" : "Non-syndromic H-type fistula"
      },
      {
        "code" : "602",
        "display" : "GNE myopathy"
      },
      {
        "code" : "603",
        "display" : "Distal myopathy, Welander type"
      },
      {
        "code" : "603448",
        "display" : "Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome"
      },
      {
        "code" : "603494",
        "display" : "Coloboma-osteopetrosis-microphthalmia-macrocephaly-albinism-deafness syndrome"
      },
      {
        "code" : "603515",
        "display" : "Isolated female hypospadias"
      },
      {
        "code" : "603684",
        "display" : "KLHL7-related Bohring-Opitz-like and Crisponi/Cold-induced sweating-like overlap syndrome"
      },
      {
        "code" : "603689",
        "display" : "KLHL7-related Bohring-Opitz-like syndrome"
      },
      {
        "code" : "603694",
        "display" : "KLHL7-related Crisponi/cold-induced sweating-like syndrome"
      },
      {
        "code" : "604680",
        "display" : "Symptomatic form of X-linked centronuclear myopathy in female carriers"
      },
      {
        "code" : "606",
        "display" : "Proximal myotonic myopathy"
      },
      {
        "code" : "609",
        "display" : "Tibial muscular dystrophy"
      },
      {
        "code" : "61",
        "display" : "Alpha-mannosidosis"
      },
      {
        "code" : "610",
        "display" : "Bethlem muscular dystrophy"
      },
      {
        "code" : "610569",
        "display" : "KIAA1109-related early lethal congenital brain malformations-arthrogryposis syndrome"
      },
      {
        "code" : "610573",
        "display" : "CLCN6-related childhood-onset progressive neurodegeneration-peripheral neuropathy syndrome"
      },
      {
        "code" : "611",
        "display" : "Inclusion body myositis"
      },
      {
        "code" : "611201",
        "display" : "Oculogastrointestinal-neurodevelopmental syndrome"
      },
      {
        "code" : "611207",
        "display" : "Spondyloepiphyseal dysplasia-sensorineural hearing loss-intellectual disability-Leber congenital amaurosis syndrome"
      },
      {
        "code" : "611216",
        "display" : "Aplastic anemia-intellectual disability-dwarfism syndrome"
      },
      {
        "code" : "611223",
        "display" : "EN1-related dorsoventral syndrome"
      },
      {
        "code" : "611237",
        "display" : "Parkinsonism with polyneuropathy"
      },
      {
        "code" : "611247",
        "display" : "Pontocerebellar hypoplasia type 11"
      },
      {
        "code" : "611256",
        "display" : "Pontocerebellar hypoplasia type 12"
      },
      {
        "code" : "613267",
        "display" : "Pontocerebellar hypoplasia type 13"
      },
      {
        "code" : "613274",
        "display" : "Pontocerebellar hypoplasia type 14"
      },
      {
        "code" : "614",
        "display" : "Thomsen and Becker disease"
      },
      {
        "code" : "615",
        "display" : "Familial atrial myxoma"
      },
      {
        "code" : "615938",
        "display" : "Spastic paraparesis-cataracts-speech delay syndrome"
      },
      {
        "code" : "615943",
        "display" : "Granuloma faciale"
      },
      {
        "code" : "615954",
        "display" : "Lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome"
      },
      {
        "code" : "615964",
        "display" : "Acute reversible leukoencephalopathy with increased urinary alpha-ketoglutarate"
      },
      {
        "code" : "615970",
        "display" : "Chronic intervillositis of unknown etiology"
      },
      {
        "code" : "615983",
        "display" : "Lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to a point mutation"
      },
      {
        "code" : "615986",
        "display" : "Lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to biallelic deletions in the ATAD3 gene cluster"
      },
      {
        "code" : "616",
        "display" : "Medulloblastoma"
      },
      {
        "code" : "616874",
        "display" : "Rare disorder without a determined diagnosis after full investigation"
      },
      {
        "code" : "617",
        "display" : "Congenital primary megaureter"
      },
      {
        "code" : "617294",
        "display" : "Twin anemia-polycythemia sequence"
      },
      {
        "code" : "617297",
        "display" : "Twin-reversed arterial perfusion sequence"
      },
      {
        "code" : "617301",
        "display" : "Selective intrauterine growth restriction"
      },
      {
        "code" : "617304",
        "display" : "Amniotic fluid embolism"
      },
      {
        "code" : "617408",
        "display" : "Classic eosinophilic pustular folliculitis"
      },
      {
        "code" : "617440",
        "display" : "Painful legs and moving toes syndrome"
      },
      {
        "code" : "617449",
        "display" : "Congenital aphakia-iris hypoplasia-microphthalmia-microcornea syndrome"
      },
      {
        "code" : "617910",
        "display" : "Conjunctival malignant melanoma"
      },
      {
        "code" : "617916",
        "display" : "Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia"
      },
      {
        "code" : "617919",
        "display" : "F12-associated cold autoinflammatory syndrome"
      },
      {
        "code" : "617930",
        "display" : "Hemophilia B Leyden"
      },
      {
        "code" : "618",
        "display" : "Familial melanoma"
      },
      {
        "code" : "618891",
        "display" : "Chronic neurovisceral acid sphingomyelinase deficiency"
      },
      {
        "code" : "619233",
        "display" : "Hereditary persistence of fetal hemoglobin-intellectual disability syndrome"
      },
      {
        "code" : "619363",
        "display" : "NOCARH syndrome"
      },
      {
        "code" : "619367",
        "display" : "SAMD9L-associated autoinflammatory syndrome"
      },
      {
        "code" : "619941",
        "display" : "Congenital neutropenia-combined immunodeficiency due to MKL1 deficiency"
      },
      {
        "code" : "619948",
        "display" : "Early-onset autoimmunity-autoinflammation-immunodeficiency syndrome due to SOCS1 haploinsufficiency"
      },
      {
        "code" : "619953",
        "display" : "Familial hyperinflammatory lymphoproliferative immunodeficiency"
      },
      {
        "code" : "619972",
        "display" : "CADINS disease"
      },
      {
        "code" : "619979",
        "display" : "Developmental delay-immunodeficiency-leukoencephalopathy-hypohomocysteinemia syndrome"
      },
      {
        "code" : "62",
        "display" : "Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3"
      },
      {
        "code" : "620102",
        "display" : "Non-syndromic unicoronal craniosynostosis"
      },
      {
        "code" : "620113",
        "display" : "Non-syndromic unilambdoid craniosynostosis"
      },
      {
        "code" : "620139",
        "display" : "Non-syndromic unifrontosphenoidal craniosynostosis"
      },
      {
        "code" : "620146",
        "display" : "Non-syndromic unisquamosal craniosynostosis"
      },
      {
        "code" : "620158",
        "display" : "Non-syndromic non-specific multisutural craniosynostosis"
      },
      {
        "code" : "620178",
        "display" : "Non-syndromic bilambdoid craniosynostosis"
      },
      {
        "code" : "620186",
        "display" : "Non-syndromic unicoronal and sagittal craniosynostosis"
      },
      {
        "code" : "620192",
        "display" : "Non-syndromic metopic and sagittal craniosynostosis"
      },
      {
        "code" : "620198",
        "display" : "Non-syndromic bicoronal and metopic craniosynostosis"
      },
      {
        "code" : "620205",
        "display" : "Non-syndromic bicoronal and sagittal craniosynostosis"
      },
      {
        "code" : "620212",
        "display" : "Non-syndromic pansynostosis"
      },
      {
        "code" : "620217",
        "display" : "Bartter syndrome type 1"
      },
      {
        "code" : "620220",
        "display" : "Bartter syndrome type 2"
      },
      {
        "code" : "620363",
        "display" : "Primary hypomagnesemia-generalized seizures-intellectual disability-obesity syndrome"
      },
      {
        "code" : "620368",
        "display" : "EGF-related primary hypomagnesemia with intellectual disability"
      },
      {
        "code" : "620371",
        "display" : "Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation"
      },
      {
        "code" : "621",
        "display" : "Hereditary methemoglobinemia"
      },
      {
        "code" : "621758",
        "display" : "Fibrosis-neurodegeneration-cerebral angiomatosis syndrome"
      },
      {
        "code" : "622",
        "display" : "Homocystinuria without methylmalonic aciduria"
      },
      {
        "code" : "622099",
        "display" : "Superior mesenteric artery syndrome"
      },
      {
        "code" : "622925",
        "display" : "X-linked severe syndromic thoracic aortic aneurysm and dissection"
      },
      {
        "code" : "622934",
        "display" : "SBDS-related severe neonatal spondylometaphyseal dysplasia"
      },
      {
        "code" : "623615",
        "display" : "Autoimmune limbic encephalitis"
      },
      {
        "code" : "623626",
        "display" : "Paraneoplastic cerebellar degeneration"
      },
      {
        "code" : "623695",
        "display" : "MIR140-related spondyloepiphyseal dysplasia"
      },
      {
        "code" : "623789",
        "display" : "Body integrity dysphoria"
      },
      {
        "code" : "623801",
        "display" : "Acute flaccid myelitis"
      },
      {
        "code" : "624",
        "display" : "Familial multiple nevi flammei"
      },
      {
        "code" : "624166",
        "display" : "Non-specific autoimmune supratentorial encephalitis with characteristic antibodies"
      },
      {
        "code" : "624178",
        "display" : "Non-specific autoimmune supratentorial encephalitis without characteristic antibodies"
      },
      {
        "code" : "624190",
        "display" : "Paraneoplastic isolated brainstem encephalitis"
      },
      {
        "code" : "624199",
        "display" : "Non-specific autoimmune brainstem encephalitis with characteristic antibodies"
      },
      {
        "code" : "624216",
        "display" : "Non-specific autoimmune brainstem encephalitis without characteristic antibodies"
      },
      {
        "code" : "624244",
        "display" : "Postinfectious cerebellitis"
      },
      {
        "code" : "624259",
        "display" : "Non-specific autoimmune cerebellar ataxia with characteristic antibodies"
      },
      {
        "code" : "624268",
        "display" : "Non-specific autoimmune cerebellar ataxia without characteristic antibodies"
      },
      {
        "code" : "626",
        "display" : "Large/giant congenital melanocytic nevus"
      },
      {
        "code" : "627",
        "display" : "Nance-Horan syndrome"
      },
      {
        "code" : "628",
        "display" : "Diastrophic dysplasia"
      },
      {
        "code" : "629",
        "display" : "Short stature due to growth hormone qualitative anomaly"
      },
      {
        "code" : "63",
        "display" : "Alport syndrome"
      },
      {
        "code" : "631",
        "display" : "Non-acquired isolated growth hormone deficiency"
      },
      {
        "code" : "631068",
        "display" : "Autosomal dominant spastic paraplegia type 80"
      },
      {
        "code" : "631073",
        "display" : "Autosomal recessive spastic paraplegia type 82"
      },
      {
        "code" : "631076",
        "display" : "Autosomal recessive spastic paraplegia type 83"
      },
      {
        "code" : "631079",
        "display" : "Autosomal recessive spastic paraplegia type 84"
      },
      {
        "code" : "631082",
        "display" : "Autosomal recessive spastic paraplegia type 85"
      },
      {
        "code" : "631085",
        "display" : "Autosomal recessive spastic paraplegia type 86"
      },
      {
        "code" : "631088",
        "display" : "Autosomal recessive spastic paraplegia type 87"
      },
      {
        "code" : "631095",
        "display" : "Spinocerebellar ataxia type 44"
      },
      {
        "code" : "631103",
        "display" : "Spinocerebellar ataxia type 48"
      },
      {
        "code" : "631106",
        "display" : "Spinocerebellar ataxia type 49"
      },
      {
        "code" : "631248",
        "display" : "Mitchell Syndrome"
      },
      {
        "code" : "631251",
        "display" : "Cancer of unknown primary site"
      },
      {
        "code" : "632",
        "display" : "Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia"
      },
      {
        "code" : "63259",
        "display" : "Iniencephaly"
      },
      {
        "code" : "63260",
        "display" : "Craniorachischisis"
      },
      {
        "code" : "632603",
        "display" : "Mesomelic dysplasia-digital anomalies-intellectual disability syndrome"
      },
      {
        "code" : "63269",
        "display" : "Antley-Bixler syndrome with genital anomaly and disorder of steroidogenesis"
      },
      {
        "code" : "63273",
        "display" : "Distal myopathy with posterior leg and anterior hand involvement"
      },
      {
        "code" : "63275",
        "display" : "Pemphigoid gestationis"
      },
      {
        "code" : "633",
        "display" : "Laron syndrome"
      },
      {
        "code" : "633004",
        "display" : "KDM3B-related intellectual disability-facial dysmorphism-short stature syndrome"
      },
      {
        "code" : "633014",
        "display" : "SLC12A2-related developmental delay-intellectual disability-sensorineural deafness syndrome"
      },
      {
        "code" : "633021",
        "display" : "SLC12A2-related autosomal recessive neonatal-developmental delay-intellectual disability-feeding difficulty-sensorineural deafness syndrome"
      },
      {
        "code" : "633024",
        "display" : "SLC12A2-related autosomal dominant infantile-developmental delay-intellectual disability-sensorineural deafness syndrome"
      },
      {
        "code" : "633028",
        "display" : "CPE-related Prader-Willi-like syndrome"
      },
      {
        "code" : "633035",
        "display" : "Intellectual disability-early-onset cataract-microcephaly syndrome"
      },
      {
        "code" : "633076",
        "display" : "Split cord malformation, composite type"
      },
      {
        "code" : "633099",
        "display" : "PAICS deficiency"
      },
      {
        "code" : "633124",
        "display" : "Invasive scopulariopsis infection"
      },
      {
        "code" : "633211",
        "display" : "Preaxial digit brachydactyly-webbed fingers"
      },
      {
        "code" : "633228",
        "display" : "Isolated proximal femoral focal deficiency"
      },
      {
        "code" : "634",
        "display" : "Netherton syndrome"
      },
      {
        "code" : "63442",
        "display" : "Angel-shaped phalango-epiphyseal dysplasia"
      },
      {
        "code" : "63446",
        "display" : "Acrocapitofemoral dysplasia"
      },
      {
        "code" : "634461",
        "display" : "Mosaic neurofibromatosis type 1"
      },
      {
        "code" : "634475",
        "display" : "Mosaic NF2-related schwannomatosis"
      },
      {
        "code" : "634492",
        "display" : "Mosaic schwannomatosis"
      },
      {
        "code" : "634511",
        "display" : "Mosaic Legius syndrome"
      },
      {
        "code" : "63455",
        "display" : "Paraneoplastic pemphigus"
      },
      {
        "code" : "635",
        "display" : "Neuroblastoma"
      },
      {
        "code" : "636",
        "display" : "Neurofibromatosis type 1"
      },
      {
        "code" : "636941",
        "display" : "Vascular Ehlers-Danlos-polymicrogyria syndrome"
      },
      {
        "code" : "636945",
        "display" : "Invasive candidiasis"
      },
      {
        "code" : "636950",
        "display" : "Glaucomatocyclitic crisis disease"
      },
      {
        "code" : "636955",
        "display" : "Endemic pemphigus foliaceus"
      },
      {
        "code" : "636965",
        "display" : "Autosomal dominant myosin storage myopathy"
      },
      {
        "code" : "636970",
        "display" : "Autosomal recessive myosin storage myopathy"
      },
      {
        "code" : "637",
        "display" : "Full NF2-related schwannomatosis"
      },
      {
        "code" : "637013",
        "display" : "SMARCA2-related blepharophimosis-intellectual disability syndrome"
      },
      {
        "code" : "637051",
        "display" : "Borna virus encephalitis"
      },
      {
        "code" : "637061",
        "display" : "Isolated optic nerve hypoplasia"
      },
      {
        "code" : "637064",
        "display" : "Isolated optic nerve aplasia"
      },
      {
        "code" : "638",
        "display" : "Neurofibromatosis-Noonan syndrome"
      },
      {
        "code" : "63862",
        "display" : "Schisis association"
      },
      {
        "code" : "63999",
        "display" : "IgG4-related mediastinitis"
      },
      {
        "code" : "64",
        "display" : "Alström syndrome"
      },
      {
        "code" : "640",
        "display" : "Hereditary neuropathy with liability to pressure palsies"
      },
      {
        "code" : "641",
        "display" : "Multifocal motor neuropathy"
      },
      {
        "code" : "641350",
        "display" : "Immunotherapy induced hypophysitis"
      },
      {
        "code" : "641353",
        "display" : "Infantile neurodegeneration-progressive spasticity-intellectual disability-white matter lesions syndrome"
      },
      {
        "code" : "641361",
        "display" : "Neurodevelopmental delay-hypotonia-cerebellar ataxia-cardiac conduction defects syndrome"
      },
      {
        "code" : "641368",
        "display" : "Autosomal recessive hyper-IgE syndrome due to ZNF341 deficiency"
      },
      {
        "code" : "641372",
        "display" : "B-lymphoblastic leukemia/lymphoma with t(7;9)(q11.2;p13.2)"
      },
      {
        "code" : "641375",
        "display" : "B-lymphoblastic leukemia/lymphoma with t(17;19)"
      },
      {
        "code" : "641380",
        "display" : "PAPASH syndrome"
      },
      {
        "code" : "641385",
        "display" : "PASS syndrome"
      },
      {
        "code" : "641390",
        "display" : "PsAPASH syndrome"
      },
      {
        "code" : "641396",
        "display" : "Central nervous system tuberculosis"
      },
      {
        "code" : "641496",
        "display" : "Childhood-onset schizophrenia"
      },
      {
        "code" : "641829",
        "display" : "Neonatal compartment syndrome"
      },
      {
        "code" : "642",
        "display" : "Hereditary sensory and autonomic neuropathy type 4"
      },
      {
        "code" : "642071",
        "display" : "Primary pulmonary vein stenosis"
      },
      {
        "code" : "642085",
        "display" : "EXOC6B-related spondyloepimetaphyseal dysplasia with joint laxity"
      },
      {
        "code" : "642099",
        "display" : "Spondyloepimetaphyseal dysplasia with joint laxity, Beighton type"
      },
      {
        "code" : "642671",
        "display" : "Familial hyperaldosteronism type IV"
      },
      {
        "code" : "642675",
        "display" : "CHD8 overgrowth syndrome"
      },
      {
        "code" : "642691",
        "display" : "Fragile X-associated primary ovarian insufficiency"
      },
      {
        "code" : "642747",
        "display" : "PUM1-related cerebellar ataxia"
      },
      {
        "code" : "642763",
        "display" : "Autosomal dominant intellectual disability-craniofacial dysmorphism-macrocephaly-hypotonia syndrome due to H1-4 mutation"
      },
      {
        "code" : "642788",
        "display" : "Cushing syndrome due to cortisol-producing adrenocortical adenoma"
      },
      {
        "code" : "64280",
        "display" : "Childhood absence epilepsy"
      },
      {
        "code" : "642945",
        "display" : "Perrault syndrome type 1"
      },
      {
        "code" : "642954",
        "display" : "Autosomal recessive ataxia due to PEX16 deficiency"
      },
      {
        "code" : "642965",
        "display" : "Autosomal recessive ataxia due to PEX2 deficiency"
      },
      {
        "code" : "642976",
        "display" : "Perrault syndrome type 2"
      },
      {
        "code" : "643",
        "display" : "Giant axonal neuropathy"
      },
      {
        "code" : "643503",
        "display" : "Marfanoid habitus-facial dysmorphism-skeletal abnormality-heart defect syndrome"
      },
      {
        "code" : "643538",
        "display" : "Hao-Fountain syndrome due to USP7 mutation"
      },
      {
        "code" : "643549",
        "display" : "Hao-Fountain syndrome"
      },
      {
        "code" : "644",
        "display" : "NARP syndrome"
      },
      {
        "code" : "645188",
        "display" : "Spinal dermal sinus"
      },
      {
        "code" : "645285",
        "display" : "Chaotic conus spinal cord lipoma"
      },
      {
        "code" : "645288",
        "display" : "Terminal extramedullary conus spinal cord lipoma"
      },
      {
        "code" : "645291",
        "display" : "Transitional extramedullary conus spinal cord lipoma"
      },
      {
        "code" : "645294",
        "display" : "Posterior extramedullary conus spinal cord lipoma"
      },
      {
        "code" : "645297",
        "display" : "Extramedullary conus spinal cord lipoma"
      },
      {
        "code" : "645300",
        "display" : "Lipomatous non-saccular limited dorsal myeloschisis"
      },
      {
        "code" : "645310",
        "display" : "Fibroneural non-saccular limited dorsal myeloschisis"
      },
      {
        "code" : "645322",
        "display" : "Isolated transitional filum lipoma"
      },
      {
        "code" : "645325",
        "display" : "Isolated filum lipoma"
      },
      {
        "code" : "645334",
        "display" : "Retained medullary cord"
      },
      {
        "code" : "645337",
        "display" : "Terminal myelocystocele"
      },
      {
        "code" : "645340",
        "display" : "Non-terminal myelocystocele"
      },
      {
        "code" : "645343",
        "display" : "Non-saccular limited dorsal myeloschisis"
      },
      {
        "code" : "645350",
        "display" : "Segmental arterial mediolysis"
      },
      {
        "code" : "645354",
        "display" : "Saccular limited dorsal myeloschisis"
      },
      {
        "code" : "645359",
        "display" : "Intramedullary non-dysraphic spinal cord lipoma"
      },
      {
        "code" : "645362",
        "display" : "Dorsal spinal cord lipoma"
      },
      {
        "code" : "645378",
        "display" : "Myelic limited dorsal malformation"
      },
      {
        "code" : "645383",
        "display" : "True myelomeningocele"
      },
      {
        "code" : "645388",
        "display" : "Hemi-myelomeningocele"
      },
      {
        "code" : "645393",
        "display" : "Hemi-myeloschisis"
      },
      {
        "code" : "645398",
        "display" : "Myeloschisis"
      },
      {
        "code" : "645401",
        "display" : "True myeloschisis"
      },
      {
        "code" : "64542",
        "display" : "Acrofacial dysostosis, Kennedy-Teebi type"
      },
      {
        "code" : "645613",
        "display" : "Classical dermatomyositis"
      },
      {
        "code" : "645617",
        "display" : "Amyopathic dermatomyositis"
      },
      {
        "code" : "645626",
        "display" : "Adermatopathic dermatomyositis"
      },
      {
        "code" : "645749",
        "display" : "Congenital esophageal stenosis"
      },
      {
        "code" : "645793",
        "display" : "Spontaneous intestinal perforation"
      },
      {
        "code" : "645807",
        "display" : "Primary tuberculous lymphadenitis"
      },
      {
        "code" : "645814",
        "display" : "Primary pulmonary tuberculosis"
      },
      {
        "code" : "645822",
        "display" : "Primary bone and joint tuberculosis"
      },
      {
        "code" : "645849",
        "display" : "Primary cutaneous tuberculosis"
      },
      {
        "code" : "645854",
        "display" : "Multifocal tuberculosis"
      },
      {
        "code" : "645859",
        "display" : "Primary tuberculosis of the digestive system"
      },
      {
        "code" : "645874",
        "display" : "Primary genito-urinary tuberculosis"
      },
      {
        "code" : "646",
        "display" : "Niemann-Pick disease type C"
      },
      {
        "code" : "646113",
        "display" : "Intermediate collagen VI-related muscular dystrophy"
      },
      {
        "code" : "646136",
        "display" : "Dysplastic cortical hyperostosis, Al-Gazali type"
      },
      {
        "code" : "646139",
        "display" : "Dysplastic cortical hyperostosis"
      },
      {
        "code" : "646278",
        "display" : "CDK13-related developmental delay-intellectual disability-facial dysmorphism-congenital heart defects syndrome"
      },
      {
        "code" : "64686",
        "display" : "Tolosa-Hunt syndrome"
      },
      {
        "code" : "64692",
        "display" : "Bartonella bacilliformis infection"
      },
      {
        "code" : "64694",
        "display" : "Trench fever"
      },
      {
        "code" : "647",
        "display" : "Nijmegen breakage syndrome"
      },
      {
        "code" : "64720",
        "display" : "Leiomyosarcoma"
      },
      {
        "code" : "64722",
        "display" : "Granulomatous mastitis"
      },
      {
        "code" : "64734",
        "display" : "Iridocorneal endothelial syndrome"
      },
      {
        "code" : "64739",
        "display" : "Ovarian hyperstimulation syndrome"
      },
      {
        "code" : "64741",
        "display" : "Pulmonary blastoma"
      },
      {
        "code" : "64742",
        "display" : "Pleuropulmonary blastoma"
      },
      {
        "code" : "64743",
        "display" : "Hepatoportal sclerosis"
      },
      {
        "code" : "64744",
        "display" : "IgG4-related thyroid disease"
      },
      {
        "code" : "64745",
        "display" : "Pruritic urticarial papules and plaques of pregnancy"
      },
      {
        "code" : "64748",
        "display" : "Dejerine-Sottas syndrome"
      },
      {
        "code" : "64751",
        "display" : "Hereditary motor and sensory neuropathy type 5"
      },
      {
        "code" : "64752",
        "display" : "Hereditary sensory and autonomic neuropathy type 5"
      },
      {
        "code" : "64753",
        "display" : "Spinocerebellar ataxia with axonal neuropathy type 2"
      },
      {
        "code" : "64754",
        "display" : "Nevus comedonicus syndrome"
      },
      {
        "code" : "64755",
        "display" : "Becker nevus syndrome"
      },
      {
        "code" : "647667",
        "display" : "Mandibuloacral dysplasia associated to MTX2"
      },
      {
        "code" : "647676",
        "display" : "Multiple epiphyseal dysplasia type 7"
      },
      {
        "code" : "647681",
        "display" : "Craniosynostosis-facial dysmorphism-Chiari-1 malformation-developmental and language delay syndrome"
      },
      {
        "code" : "647772",
        "display" : "Isolated primary pigmented nodular adrenocortical disease"
      },
      {
        "code" : "647782",
        "display" : "Isolated micronodular adrenocortical disease"
      },
      {
        "code" : "647788",
        "display" : "Neurodevelopmental delay-intellectual disability-ataxia-feeding difficulty syndrome"
      },
      {
        "code" : "647794",
        "display" : "Isolated persistent urogenital sinus"
      },
      {
        "code" : "647799",
        "display" : "MYT1L-related developmental delay-intellectual disability-obesity syndrome"
      },
      {
        "code" : "647804",
        "display" : "Combined immunodeficiency due to FCHO1 deficiency"
      },
      {
        "code" : "647811",
        "display" : "Cardiac-urogenital syndrome"
      },
      {
        "code" : "647815",
        "display" : "Keratitis fugax hereditaria"
      },
      {
        "code" : "647823",
        "display" : "Idiopathic pregnancy-associated osteoporosis"
      },
      {
        "code" : "647834",
        "display" : "SLC40A1-related hemochromatosis"
      },
      {
        "code" : "647916",
        "display" : "Conjoined twins"
      },
      {
        "code" : "648",
        "display" : "Noonan syndrome"
      },
      {
        "code" : "648562",
        "display" : "Ferroportin disease"
      },
      {
        "code" : "648581",
        "display" : "Digenic hemochromatosis"
      },
      {
        "code" : "648665",
        "display" : "Infectious scleritis"
      },
      {
        "code" : "648675",
        "display" : "Idiopathic scleritis"
      },
      {
        "code" : "648681",
        "display" : "Immune-mediated scleritis"
      },
      {
        "code" : "648684",
        "display" : "Central retinal artery occlusion"
      },
      {
        "code" : "648919",
        "display" : "Idiopathic catatonia"
      },
      {
        "code" : "648992",
        "display" : "Non-syndromic bridging bronchus"
      },
      {
        "code" : "649",
        "display" : "Norrie disease"
      },
      {
        "code" : "649010",
        "display" : "Non-syndromic congenital bronchial atresia"
      },
      {
        "code" : "649029",
        "display" : "Isolated left bronchial isomerism"
      },
      {
        "code" : "65",
        "display" : "Leber congenital amaurosis"
      },
      {
        "code" : "650",
        "display" : "LCAT deficiency"
      },
      {
        "code" : "650077",
        "display" : "Genetic central precocious puberty in female"
      },
      {
        "code" : "650082",
        "display" : "Secondary central precocious puberty in female"
      },
      {
        "code" : "650087",
        "display" : "Primary central precocious puberty in male"
      },
      {
        "code" : "650092",
        "display" : "Secondary central precocious puberty in male"
      },
      {
        "code" : "650097",
        "display" : "Genetic central precocious puberty in male"
      },
      {
        "code" : "650102",
        "display" : "Non-genetic central precocious puberty in male"
      },
      {
        "code" : "652",
        "display" : "Multiple endocrine neoplasia type 1"
      },
      {
        "code" : "652487",
        "display" : "Developmental delay-overweight-facial dysmorphism-behavioral abnormalities syndrome"
      },
      {
        "code" : "652514",
        "display" : "Cleft palate-congenital heart defect-intellectual disability syndrome due to MEIS2 mutation"
      },
      {
        "code" : "652519",
        "display" : "Cleft palate-congenital heart defect-intellectual disability syndrome"
      },
      {
        "code" : "652522",
        "display" : "Periodic fever-immunodeficiency-thrombocytopenia syndrome"
      },
      {
        "code" : "652528",
        "display" : "Non-syndromic supernumerary kidneys"
      },
      {
        "code" : "652532",
        "display" : "Adult-onset progressive leukoencephalopathy-early-onset deafness"
      },
      {
        "code" : "652650",
        "display" : "Nodal T-follicular helper cell lymphoma, follicular type"
      },
      {
        "code" : "652658",
        "display" : "Monomorphic epitheliotropic intestinal T-cell lymphoma"
      },
      {
        "code" : "652668",
        "display" : "Primary superior vena cava aneurysm"
      },
      {
        "code" : "652678",
        "display" : "Primary inferior vena cava aneurysm"
      },
      {
        "code" : "652681",
        "display" : "Idiopathic subglottic stenosis"
      },
      {
        "code" : "65282",
        "display" : "Carvajal syndrome"
      },
      {
        "code" : "65283",
        "display" : "Timothy syndrome"
      },
      {
        "code" : "65284",
        "display" : "Biotin-thiamine-responsive basal ganglia disease"
      },
      {
        "code" : "65285",
        "display" : "Lhermitte-Duclos disease"
      },
      {
        "code" : "65286",
        "display" : "3q29 microdeletion syndrome"
      },
      {
        "code" : "65287",
        "display" : "Beta-ureidopropionase deficiency"
      },
      {
        "code" : "65288",
        "display" : "Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome"
      },
      {
        "code" : "653",
        "display" : "Multiple endocrine neoplasia type 2"
      },
      {
        "code" : "653698",
        "display" : "Lymphocytic mastitis"
      },
      {
        "code" : "653709",
        "display" : "Cone rod dystrophy-short stature syndrome"
      },
      {
        "code" : "653712",
        "display" : "CHD4-related neurodevelopmental disorder"
      },
      {
        "code" : "653722",
        "display" : "Digenic Alport syndrome"
      },
      {
        "code" : "653725",
        "display" : "Autosomal recessive limb-girdle muscular dystrophy, type 28"
      },
      {
        "code" : "653728",
        "display" : "Congenital insensitivity to pain syndrome, Marsili type"
      },
      {
        "code" : "653751",
        "display" : "X-linked combined immunodeficiency due to SASH3 deficiency"
      },
      {
        "code" : "653767",
        "display" : "Jansen-de Vries syndrome"
      },
      {
        "code" : "653880",
        "display" : "Mitochondrial short-chain enoyl-CoA hydratase 1 deficiency"
      },
      {
        "code" : "654",
        "display" : "Nephroblastoma"
      },
      {
        "code" : "655",
        "display" : "Nephronophthisis"
      },
      {
        "code" : "656",
        "display" : "Hereditary steroid-resistant nephrotic syndrome"
      },
      {
        "code" : "656071",
        "display" : "Atrophic papulosis"
      },
      {
        "code" : "656085",
        "display" : "Benign atrophic papulosis"
      },
      {
        "code" : "656126",
        "display" : "Segmental spinal dysgenesis"
      },
      {
        "code" : "656130",
        "display" : "PBX1-related congenital anomalies of kidney-urinary tract syndrome"
      },
      {
        "code" : "656135",
        "display" : "Intellectual disability-cupped ears syndrome"
      },
      {
        "code" : "656279",
        "display" : "1p36.33 duplication syndrome"
      },
      {
        "code" : "656283",
        "display" : "Autosomal recessive combined immunodeficiency due to complete IL6ST deficiency"
      },
      {
        "code" : "656300",
        "display" : "Autosomal recessive combined immunodeficiency due to partial IL6ST deficiency"
      },
      {
        "code" : "656313",
        "display" : "Autosomal dominant combined immunodeficiency due to partial IL6ST deficiency"
      },
      {
        "code" : "656326",
        "display" : "Autosomal recessive combined immunodeficiency due to IL6R deficiency"
      },
      {
        "code" : "656417",
        "display" : "Embryonal tumor with multilayered rosettes"
      },
      {
        "code" : "65681",
        "display" : "Vaginal atresia"
      },
      {
        "code" : "65682",
        "display" : "Benign recurrent intrahepatic cholestasis"
      },
      {
        "code" : "65683",
        "display" : "Isolated focal cortical dysplasia"
      },
      {
        "code" : "65684",
        "display" : "Monomelic amyotrophy"
      },
      {
        "code" : "656912",
        "display" : "Autosomal dominant combined immunodeficiency due to ERBIN deficiency"
      },
      {
        "code" : "65720",
        "display" : "Arthrogryposis-severe scoliosis syndrome"
      },
      {
        "code" : "65743",
        "display" : "Autosomal dominant multiple pterygium syndrome"
      },
      {
        "code" : "65748",
        "display" : "Multiple self-healing squamous epithelioma"
      },
      {
        "code" : "65759",
        "display" : "Carpenter syndrome"
      },
      {
        "code" : "658540",
        "display" : "16q22 deletion syndrome"
      },
      {
        "code" : "658549",
        "display" : "Idiopathic small fibers neuropathy"
      },
      {
        "code" : "658574",
        "display" : "Isolated pulmonary artery sling"
      },
      {
        "code" : "658584",
        "display" : "Rowell syndrome"
      },
      {
        "code" : "658590",
        "display" : "Eyelid sebaceous carcinoma"
      },
      {
        "code" : "658595",
        "display" : "DNMT3A-related microcephalic dwarfism"
      },
      {
        "code" : "658602",
        "display" : "Transplant-related bronchiolitis obliterans"
      },
      {
        "code" : "658612",
        "display" : "Non-transplant-related bronchiolitis obliterans"
      },
      {
        "code" : "658778",
        "display" : "COQ7-related distal hereditary motor neuropathy"
      },
      {
        "code" : "658805",
        "display" : "Greig cephalopolysyndactyly-contiguous gene syndrome"
      },
      {
        "code" : "658810",
        "display" : "Atrophoderma of Pasini and Pierini"
      },
      {
        "code" : "658813",
        "display" : "Combined immunodeficiency-megaloblastic anemia due to methylenetetrahydrofolate dehydrogenase 1 deficiency"
      },
      {
        "code" : "658843",
        "display" : "Developmental delay-ataxia-hypotonia-facial dysmorphism syndrome"
      },
      {
        "code" : "658909",
        "display" : "Fasciolopsiasis"
      },
      {
        "code" : "658913",
        "display" : "Paragonimiasis"
      },
      {
        "code" : "658917",
        "display" : "Clonorchiasis"
      },
      {
        "code" : "658946",
        "display" : "Early-onset immune dysregulation with autoimmunity due to DOCK11 partial deficiency"
      },
      {
        "code" : "658951",
        "display" : "Early-onset immune dysregulation due to DOCK11 complete deficiency"
      },
      {
        "code" : "659",
        "display" : "Mutilating palmoplantar keratoderma with periorificial keratotic plaques"
      },
      {
        "code" : "659396",
        "display" : "Cohen-Gibson syndrome"
      },
      {
        "code" : "659463",
        "display" : "Imagawa-Matsumoto syndrome"
      },
      {
        "code" : "659609",
        "display" : "Facial dysmorphism-global developmental delay-hypotonia-polymicrogyria syndrome"
      },
      {
        "code" : "659626",
        "display" : "Single isolated optic neuritis"
      },
      {
        "code" : "659634",
        "display" : "Relapsing isolated optic neuritis"
      },
      {
        "code" : "659642",
        "display" : "Rauch-Steindl syndrome"
      },
      {
        "code" : "659672",
        "display" : "Harderoporphyria"
      },
      {
        "code" : "659702",
        "display" : "Intrauterine growth retardation-micrognathia-short stature-facial dysmorphism-rhizomelic shortening syndrome"
      },
      {
        "code" : "659707",
        "display" : "Yersinia pseudotuberculosis infection"
      },
      {
        "code" : "659744",
        "display" : "Ocular surface squamous neoplasia"
      },
      {
        "code" : "659756",
        "display" : "Oroya fever"
      },
      {
        "code" : "659759",
        "display" : "Verruga peruana"
      },
      {
        "code" : "659873",
        "display" : "Wormian bones-micrognathia-abnormal dentition-progeroid syndrome"
      },
      {
        "code" : "659904",
        "display" : "Multiple congenital anomalies-neurodevelopmental delay-ocular abnormalities syndrome"
      },
      {
        "code" : "659908",
        "display" : "Glanders"
      },
      {
        "code" : "659975",
        "display" : "Sensorineural hearing loss-spastic quadriplegia-intellectual disability syndrome"
      },
      {
        "code" : "660",
        "display" : "Omphalocele"
      },
      {
        "code" : "660012",
        "display" : "Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to a NR4A2 point mutation"
      },
      {
        "code" : "660017",
        "display" : "Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome"
      },
      {
        "code" : "660021",
        "display" : "Orofacial clefting-cardiac anomalies-facial dysmorphism syndrome"
      },
      {
        "code" : "660053",
        "display" : "Psittacosis"
      },
      {
        "code" : "661",
        "display" : "Congenital central hypoventilation syndrome"
      },
      {
        "code" : "661412",
        "display" : "Megaloblastic anemia-immunodeficiency due to folate transporter 1 deficiency"
      },
      {
        "code" : "661526",
        "display" : "MBD4-related tumor predisposition syndrome"
      },
      {
        "code" : "662",
        "display" : "Lymphedema with yellow nails"
      },
      {
        "code" : "662169",
        "display" : "Phelan-McDermid syndrome due to 22q13.3 deletion"
      },
      {
        "code" : "662172",
        "display" : "Phelan-McDermid syndrome due to SHANK3 mutation"
      },
      {
        "code" : "662175",
        "display" : "Macrocephaly-congenital heart disease-facial dysmorphism-intellectual disability syndrome"
      },
      {
        "code" : "662179",
        "display" : "Microcephaly-hearing loss-facial dysmorphism-intellectual disability syndrome"
      },
      {
        "code" : "662184",
        "display" : "Congenital muscular dystrophy-cataract-intellectual disability syndrome"
      },
      {
        "code" : "662189",
        "display" : "Neurodevelopmental disorder-brain malformation-facial dysmorphism-brachydactyly syndrome"
      },
      {
        "code" : "662198",
        "display" : "Neurodevelopmental delay-intellectual disability-skeletal defects syndrome"
      },
      {
        "code" : "662207",
        "display" : "Neurodevelopmental delay-brain malformations-skeletal defects-intellectual disability syndrome"
      },
      {
        "code" : "662216",
        "display" : "Mucopolysaccharidosis type 10"
      },
      {
        "code" : "662229",
        "display" : "Episodic memory defect leukoencephalopathy"
      },
      {
        "code" : "662234",
        "display" : "Neurodevelopmental delay-congenital heart defects-intellectual disability syndrome"
      },
      {
        "code" : "662240",
        "display" : "Frey syndrome"
      },
      {
        "code" : "662255",
        "display" : "Grisel syndrome"
      },
      {
        "code" : "662367",
        "display" : "NESCAV syndrome"
      },
      {
        "code" : "662376",
        "display" : "Isolated gastric duplication"
      },
      {
        "code" : "662388",
        "display" : "Isolated gallbladder duplication"
      },
      {
        "code" : "662392",
        "display" : "Isolated colonic duplication"
      },
      {
        "code" : "662405",
        "display" : "Isolated pyloric duplication"
      },
      {
        "code" : "662456",
        "display" : "Isolated small intestine duplication"
      },
      {
        "code" : "662473",
        "display" : "Isolated duodenal duplication"
      },
      {
        "code" : "662480",
        "display" : "Isolated jejuno-ileal duplication"
      },
      {
        "code" : "662721",
        "display" : "Placenta accreta spectrum disorder"
      },
      {
        "code" : "662762",
        "display" : "Motor delay-microcephaly-speech impairment-ocular abnormalities syndrome"
      },
      {
        "code" : "662786",
        "display" : "Vasa previa"
      },
      {
        "code" : "662829",
        "display" : "Intellectual disability-speech delay-dysmorphic features-T cell abnormalities syndrome"
      },
      {
        "code" : "662934",
        "display" : "Acute megakaryoblastic leukemia in adult"
      },
      {
        "code" : "663",
        "display" : "Mitochondrial DNA-related progressive external ophthalmoplegia"
      },
      {
        "code" : "664",
        "display" : "Ornithine transcarbamylase deficiency"
      },
      {
        "code" : "664372",
        "display" : "Soft and hard cleft palate"
      },
      {
        "code" : "664377",
        "display" : "MGP-related spondyloepiphyseal dysplasia"
      },
      {
        "code" : "664401",
        "display" : "Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome due to TAB2 mutation"
      },
      {
        "code" : "664404",
        "display" : "6q25.1 microdeletion syndrome"
      },
      {
        "code" : "664410",
        "display" : "Brain abnormalities-severe developmental delay-facial dysmorphism-intellectual disability syndrome"
      },
      {
        "code" : "664416",
        "display" : "Brain abnormalities-severe developmental delay-facial dysmorphism-intellectual disability syndrome due to MEF2C mutation"
      },
      {
        "code" : "664430",
        "display" : "Neurodevelopmental disorder-slit-like lateral ventricles-intellectual disability syndrome"
      },
      {
        "code" : "664438",
        "display" : "Gingival fibromatosis-aortic root dilatation-facial dysmorphism-intellectual disability syndrome"
      },
      {
        "code" : "664500",
        "display" : "Hermansky-Pudlak syndrome due to AP3B1 deficiency"
      },
      {
        "code" : "664511",
        "display" : "Early-onset severe Hermansky-Pudlak syndrome with hearing loss, due to AP3D1 deficiency"
      },
      {
        "code" : "664699",
        "display" : "EBV-induced lymphoproliferative disease due to RASGRP1 deficiency"
      },
      {
        "code" : "664711",
        "display" : "EBV-induced lymphoproliferative disease due to PRKCD deficiency"
      },
      {
        "code" : "664726",
        "display" : "EBV-induced lymphoproliferative disease due to CD137 deficiency"
      },
      {
        "code" : "664729",
        "display" : "EBV-induced lymphoproliferative disease due to TET2 deficiency"
      },
      {
        "code" : "664787",
        "display" : "Nicolau syndrome"
      },
      {
        "code" : "664901",
        "display" : "Trigeminal trophic syndrome"
      },
      {
        "code" : "664912",
        "display" : "Neonatal renal venous thrombosis"
      },
      {
        "code" : "664923",
        "display" : "Congenital arthrogryposis-microcephaly-facial dysmorphism-severe neurodevelopmental delay syndrome"
      },
      {
        "code" : "665044",
        "display" : "Common arterial trunk with aortic dominance"
      },
      {
        "code" : "665058",
        "display" : "Common arterial trunk with pulmonary dominance and interrupted aortic arch"
      },
      {
        "code" : "66518",
        "display" : "Short fifth metacarpals-insulin resistance syndrome"
      },
      {
        "code" : "66529",
        "display" : "Tako-Tsubo cardiomyopathy"
      },
      {
        "code" : "666",
        "display" : "Osteogenesis imperfecta"
      },
      {
        "code" : "66624",
        "display" : "PANDAS"
      },
      {
        "code" : "66625",
        "display" : "Cerebrooculonasal syndrome"
      },
      {
        "code" : "66627",
        "display" : "Tenosynovial giant cell tumor"
      },
      {
        "code" : "66628",
        "display" : "Obesity due to congenital leptin deficiency"
      },
      {
        "code" : "66629",
        "display" : "Goldberg-Shprintzen megacolon syndrome"
      },
      {
        "code" : "66630",
        "display" : "Congenital pseudoarthrosis of the clavicle"
      },
      {
        "code" : "66631",
        "display" : "CEDNIK syndrome"
      },
      {
        "code" : "66633",
        "display" : "Sensorineural hearing loss-early graying-essential tremor syndrome"
      },
      {
        "code" : "66634",
        "display" : "Dilated cardiomyopathy with ataxia"
      },
      {
        "code" : "66637",
        "display" : "Diaphanospondylodysostosis"
      },
      {
        "code" : "66661",
        "display" : "Mast cell sarcoma"
      },
      {
        "code" : "66662",
        "display" : "Extracutaneous mastocytoma"
      },
      {
        "code" : "667",
        "display" : "Autosomal recessive malignant osteopetrosis"
      },
      {
        "code" : "667589",
        "display" : "Isolated congenital femoral bifurcation"
      },
      {
        "code" : "667662",
        "display" : "Breast implant-associated anaplastic large cell lymphoma"
      },
      {
        "code" : "667678",
        "display" : "Intraoral basal cell carcinoma"
      },
      {
        "code" : "668",
        "display" : "Osteosarcoma"
      },
      {
        "code" : "67",
        "display" : "Amoebiasis due to Entamoeba histolytica"
      },
      {
        "code" : "67036",
        "display" : "Autosomal dominant optic atrophy and cataract"
      },
      {
        "code" : "67038",
        "display" : "B-cell chronic lymphocytic leukemia"
      },
      {
        "code" : "67039",
        "display" : "Segmental odontomaxillary dysplasia"
      },
      {
        "code" : "67041",
        "display" : "Hyaluronidase deficiency"
      },
      {
        "code" : "67042",
        "display" : "Late-onset retinal degeneration"
      },
      {
        "code" : "67043",
        "display" : "Amoebic keratitis"
      },
      {
        "code" : "67044",
        "display" : "Thrombocytopenia with congenital dyserythropoietic anemia"
      },
      {
        "code" : "67045",
        "display" : "X-linked intellectual disability with isolated growth hormone deficiency"
      },
      {
        "code" : "67046",
        "display" : "3-methylglutaconic aciduria type 1"
      },
      {
        "code" : "67047",
        "display" : "3-methylglutaconic aciduria type 3"
      },
      {
        "code" : "67048",
        "display" : "3-methylglutaconic aciduria type 4"
      },
      {
        "code" : "672",
        "display" : "Pallister-Hall syndrome"
      },
      {
        "code" : "672979",
        "display" : "Craniosynostosis-facial dysmorphism-brachydactyly syndrome"
      },
      {
        "code" : "672985",
        "display" : "Craniosynostosis-skeletal and cerebellar anomalies-learning disabilities syndrome"
      },
      {
        "code" : "673",
        "display" : "Malaria"
      },
      {
        "code" : "673525",
        "display" : "Intravascular papillary endothelial hyperplasia"
      },
      {
        "code" : "673538",
        "display" : "Littoral cell hemangioma of the spleen"
      },
      {
        "code" : "673543",
        "display" : "Papillary hemangioma"
      },
      {
        "code" : "673556",
        "display" : "Pseudomyogenic hemangioendothelioma"
      },
      {
        "code" : "673568",
        "display" : "Eccrine angiomatous hamartoma"
      },
      {
        "code" : "673574",
        "display" : "Reactive angioendotheliomatosis"
      },
      {
        "code" : "673580",
        "display" : "Classic pilocytic astrocytoma"
      },
      {
        "code" : "673585",
        "display" : "Pilocytic astrocytoma with histological features of anaplasia"
      },
      {
        "code" : "674",
        "display" : "Accessory pancreas"
      },
      {
        "code" : "674653",
        "display" : "Actinomyopathy-associated syndromic thrombocytopenia"
      },
      {
        "code" : "674762",
        "display" : "Early-onset autoinflammatory syndrome due to A20 haploinsufficiency"
      },
      {
        "code" : "674924",
        "display" : "Isolated retinal racemose hemangioma"
      },
      {
        "code" : "674930",
        "display" : "Perifoveal exudative vascular anomalous complex"
      },
      {
        "code" : "674935",
        "display" : "Torpedo Maculopathy"
      },
      {
        "code" : "674943",
        "display" : "Isolated angioid streaks"
      },
      {
        "code" : "674947",
        "display" : "Diffuse unilateral subacute neuroretinitis"
      },
      {
        "code" : "674953",
        "display" : "Multiple evanescent white dot syndrome"
      },
      {
        "code" : "674958",
        "display" : "Stellate multiform amelanotic choroidopathy"
      },
      {
        "code" : "674965",
        "display" : "Choroidal osteoma"
      },
      {
        "code" : "674968",
        "display" : "Bilateral diffuse uveal melanocytic proliferation disease"
      },
      {
        "code" : "675",
        "display" : "Annular pancreas"
      },
      {
        "code" : "675216",
        "display" : "Spinocerebellar ataxia type 27B"
      },
      {
        "code" : "675359",
        "display" : "Anastomosing haemangioma"
      },
      {
        "code" : "675362",
        "display" : "Hobnail hemangioma"
      },
      {
        "code" : "675369",
        "display" : "Microvenular haemangioma"
      },
      {
        "code" : "675380",
        "display" : "Isolated segmental infantile hemangioma"
      },
      {
        "code" : "675396",
        "display" : "Epithelioid hemangioma"
      },
      {
        "code" : "675404",
        "display" : "May-Thurner syndrome"
      },
      {
        "code" : "675597",
        "display" : "Acquired elastotic haemangioma"
      },
      {
        "code" : "675628",
        "display" : "TLR8-related inflammation-severe neutropenia-bone marrow failure-lymphoproliferation syndrome"
      },
      {
        "code" : "675767",
        "display" : "Severe congenital neutropenia-developmental delay syndrome due to SRP54 deficiency"
      },
      {
        "code" : "675775",
        "display" : "Severe congenital myelofibrosis-pancytopenia-intellectual disability-neurologic and ophthalmic abnormalities syndrome"
      },
      {
        "code" : "675782",
        "display" : "Progressive hypotonia-intellectual disability-facial dysmorphism syndrome due to FYVE-defective RBSN"
      },
      {
        "code" : "675814",
        "display" : "Adenomatoid tumour of the pleura"
      },
      {
        "code" : "675822",
        "display" : "Well-differentiated papillary mesothelial tumour of the pleura"
      },
      {
        "code" : "675833",
        "display" : "Localized pleural mesothelioma"
      },
      {
        "code" : "675837",
        "display" : "Diffused pleural mesothelioma"
      },
      {
        "code" : "675841",
        "display" : "Pleural mesothelioma in situ"
      },
      {
        "code" : "675976",
        "display" : "Adenomatoid tumour of the peritoneum"
      },
      {
        "code" : "676",
        "display" : "Autosomal dominant hereditary chronic pancreatitis"
      },
      {
        "code" : "676033",
        "display" : "Well-differentiated papillary mesothelial tumour of the peritoneum"
      },
      {
        "code" : "676036",
        "display" : "Peritoneal mesothelioma in situ"
      },
      {
        "code" : "676039",
        "display" : "Combined immunodeficiency due to FOXN1 haploinsufficiency"
      },
      {
        "code" : "676125",
        "display" : "X-linked immune dysregulation with inflammatory bowel disease due to ELF4 deficiency"
      },
      {
        "code" : "677",
        "display" : "Pancreatoblastoma"
      },
      {
        "code" : "678",
        "display" : "Papillon-Lefèvre syndrome"
      },
      {
        "code" : "679",
        "display" : "Malignant atrophic papulosis"
      },
      {
        "code" : "68",
        "display" : "Amoebiasis due to free-living amoebae"
      },
      {
        "code" : "681",
        "display" : "Hypokalemic periodic paralysis"
      },
      {
        "code" : "682",
        "display" : "Hyperkalemic periodic paralysis"
      },
      {
        "code" : "683",
        "display" : "Progressive supranuclear palsy"
      },
      {
        "code" : "684",
        "display" : "Paramyotonia congenita of Von Eulenburg"
      },
      {
        "code" : "684216",
        "display" : "Intellectual disability-facial dysmorphism-joint hypermobility-hearing loss syndrome"
      },
      {
        "code" : "684226",
        "display" : "Intellectual disability-hypotonia-facial dysmorphism-macrocephaly syndrome"
      },
      {
        "code" : "684232",
        "display" : "Intellectual disability-épilepsy-dental anomalies-facial dysmorphism syndrome"
      },
      {
        "code" : "684240",
        "display" : "Neurodevelopmental disorder-spasticity-movement disorder-epileptic syndrome"
      },
      {
        "code" : "684247",
        "display" : "Isolated growth hormone deficiency type IV"
      },
      {
        "code" : "684290",
        "display" : "Hypertrophic olivary degeneration"
      },
      {
        "code" : "684305",
        "display" : "Neurooculocardiogenitourinary syndrome"
      },
      {
        "code" : "684742",
        "display" : "2q13 microdeletion syndrome"
      },
      {
        "code" : "684752",
        "display" : "Isolated anal canal duplication"
      },
      {
        "code" : "685004",
        "display" : "Primary pericardial mesothelioma"
      },
      {
        "code" : "685010",
        "display" : "Mesothelioma of the tunica vaginalis"
      },
      {
        "code" : "685017",
        "display" : "Combined immunodeficiency due to TBX1 deficiency"
      },
      {
        "code" : "685067",
        "display" : "Hypodontia-scalp hypotrichosis-facial dysmorphism syndrome"
      },
      {
        "code" : "685082",
        "display" : "Pediatric acute respiratory distress syndrome"
      },
      {
        "code" : "686462",
        "display" : "Non-fibrotic hypersensitivity pneumonitis"
      },
      {
        "code" : "686465",
        "display" : "Fibrotic hypersensitivity pneumonitis"
      },
      {
        "code" : "686468",
        "display" : "Post 5-alpha-reductase inhibitors treatment syndrome"
      },
      {
        "code" : "686475",
        "display" : "Post-selective serotonin reuptake inhibitor sexual dysfunction"
      },
      {
        "code" : "686482",
        "display" : "BPTF-related intellectual disability-facial dysmorphism-skeletal anomalies syndrome"
      },
      {
        "code" : "686488",
        "display" : "RNU4-2-related neurodevelopmental disorder-facial dysmorphism-white matter abnormalities-short stature syndrome"
      },
      {
        "code" : "686495",
        "display" : "MADD-related developmental delay-endocrine dysfunction-hypohemoglobinemia syndrome"
      },
      {
        "code" : "686556",
        "display" : "Isolated congenital cholesteatoma of the middle ear"
      },
      {
        "code" : "686999",
        "display" : "Lipodystrophy-demyelinating peripheral sensory-motor neuropathy syndrome"
      },
      {
        "code" : "687424",
        "display" : "ZMYND11-related developmental delay-speech delay-seizures-behavioral abnormalities-craniofacial dysmorphism syndrome due to 10p15.3 microdeletion"
      },
      {
        "code" : "687695",
        "display" : "10p13-p14 deletion syndrome"
      },
      {
        "code" : "687730",
        "display" : "Unifocal Langerhans cell histiocytosis"
      },
      {
        "code" : "687733",
        "display" : "Pulmonary Langerhans cell histiocytosis"
      },
      {
        "code" : "687738",
        "display" : "Single-system multifocal Langerhans cell histiocytosis"
      },
      {
        "code" : "687741",
        "display" : "Multisystem Langerhans cell histiocytosis"
      },
      {
        "code" : "688523",
        "display" : "Splenic venous malformation"
      },
      {
        "code" : "688543",
        "display" : "Reticular dysgenesis-like severe combined immunodeficiency"
      },
      {
        "code" : "688581",
        "display" : "Midface hypoplasia-hearing impairment-elliptocytosis-nephrocalcinosis syndrome"
      },
      {
        "code" : "688594",
        "display" : "Combined immunodeficiency due to RELB deficiency"
      },
      {
        "code" : "688642",
        "display" : "Turnpenny-Fry syndrome"
      },
      {
        "code" : "688649",
        "display" : "Isolated adrenal medullary hyperplasia"
      },
      {
        "code" : "688995",
        "display" : "Scarlet fever"
      },
      {
        "code" : "689001",
        "display" : "Isolated spontaneous cervical artery dissection"
      },
      {
        "code" : "689021",
        "display" : "Asymptomatic hyperCKemia-myalgia-rhabdomyolysis syndrome"
      },
      {
        "code" : "689231",
        "display" : "IFIH1-related hereditary spastic paraplegia"
      },
      {
        "code" : "689234",
        "display" : "RNASEH2B-related hereditary spastic paraplegia"
      },
      {
        "code" : "689397",
        "display" : "Poirier-Bienvenu neurodevelopmental syndrome"
      },
      {
        "code" : "689401",
        "display" : "Acquired hypothalamic obesity"
      },
      {
        "code" : "689408",
        "display" : "Shashi-Pena syndrome"
      },
      {
        "code" : "689422",
        "display" : "Okur-Chung neurodevelopmental syndrome"
      },
      {
        "code" : "689430",
        "display" : "Adenoid ameloblastoma"
      },
      {
        "code" : "689822",
        "display" : "Structural heart defects-renal anomalies syndrome"
      },
      {
        "code" : "689829",
        "display" : "Microphthalmia-motor delay-language delay-brain anomalies-diaphragmatic hernia syndrome"
      },
      {
        "code" : "69061",
        "display" : "Idiopathic steroid-sensitive nephrotic syndrome"
      },
      {
        "code" : "69063",
        "display" : "Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization"
      },
      {
        "code" : "69076",
        "display" : "Familial renal glucosuria"
      },
      {
        "code" : "69077",
        "display" : "Rhabdoid tumor"
      },
      {
        "code" : "69078",
        "display" : "Liposarcoma"
      },
      {
        "code" : "69082",
        "display" : "Odonto-tricho-ungual-digito-palmar syndrome"
      },
      {
        "code" : "69083",
        "display" : "Ectodermal dysplasia with natal teeth, Turnpenny type"
      },
      {
        "code" : "69084",
        "display" : "Pure hair and nail ectodermal dysplasia"
      },
      {
        "code" : "69085",
        "display" : "Limb-mammary syndrome"
      },
      {
        "code" : "69087",
        "display" : "Naegeli-Franceschetti-Jadassohn syndrome"
      },
      {
        "code" : "69088",
        "display" : "Hypohidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome"
      },
      {
        "code" : "69125",
        "display" : "Anonychia with flexural pigmentation"
      },
      {
        "code" : "69126",
        "display" : "PAPA syndrome"
      },
      {
        "code" : "692173",
        "display" : "Marbach-Schaaf neurodevelopmental syndrome"
      },
      {
        "code" : "692193",
        "display" : "CHAMP1-related intellectual disability-facial dysmorphism-behavioral abnormalities syndrome"
      },
      {
        "code" : "692256",
        "display" : "Isolated anogenital granulomatosis"
      },
      {
        "code" : "692271",
        "display" : "Cerebral proliferative angiopathy"
      },
      {
        "code" : "692296",
        "display" : "Idiopathic triglyceride deposit cardiomyovasculopathy"
      },
      {
        "code" : "692305",
        "display" : "Triglyceride deposit cardiomyovasculopathy"
      },
      {
        "code" : "692790",
        "display" : "ATP6AP1-CDG"
      },
      {
        "code" : "692812",
        "display" : "RAC2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndrome"
      },
      {
        "code" : "693549",
        "display" : "Facial dysmorphism-Intellectual disability-rhombencephalosynapsis syndrome"
      },
      {
        "code" : "693627",
        "display" : "Agammaglobulinemia-skin involvement-failure to thrive syndrome"
      },
      {
        "code" : "693647",
        "display" : "Agammaglobulinemia-early-onset hypertrophic cardiomyopathy-neutropenia syndrome"
      },
      {
        "code" : "693661",
        "display" : "Activated PI3K-delta syndrome 1"
      },
      {
        "code" : "693681",
        "display" : "Activated PI3K-delta syndrome 2"
      },
      {
        "code" : "693815",
        "display" : "Uterine arteriovenous malformation"
      },
      {
        "code" : "693826",
        "display" : "Pancreatic arteriovenous malformation"
      },
      {
        "code" : "693832",
        "display" : "Gastrointestinal tract arteriovenous malformation"
      },
      {
        "code" : "693839",
        "display" : "Renal arteriovenous malformation"
      },
      {
        "code" : "693846",
        "display" : "Hepatic arteriovenous malformation"
      },
      {
        "code" : "693863",
        "display" : "Splenic arteriovenous malformation"
      },
      {
        "code" : "693869",
        "display" : "Gallblader arteriovenous malformation"
      },
      {
        "code" : "693872",
        "display" : "Urinary tract arteriovenous malformation"
      },
      {
        "code" : "693907",
        "display" : "RASA1-related capillary malformation-arteriovenous malformation"
      },
      {
        "code" : "693912",
        "display" : "EPHB4-related capillary malformation-arteriovenous malformation"
      },
      {
        "code" : "694228",
        "display" : "Congenital intrahepatic arterioportal fistula"
      },
      {
        "code" : "694304",
        "display" : "ZMYND11-related developmental delay-speech delay-seizures-behavioral abnormalities-craniofacial dysmorphism syndrome"
      },
      {
        "code" : "694308",
        "display" : "ZMYND11-related developmental delay-speech delay-seizures-behavioral abnormalities-craniofacial dysmorphism syndrome due to a point mutation"
      },
      {
        "code" : "694356",
        "display" : "ADAR-related hereditary spastic paraplegia"
      },
      {
        "code" : "694922",
        "display" : "Childhood-onset stress-induced neurodegenerative ataxia-seizure syndrome"
      },
      {
        "code" : "694937",
        "display" : "Intellectual disability-peripheral neuropathy-corpus callosum abnormalities syndrome due to nudix hydrolase 2 deficiency"
      },
      {
        "code" : "694946",
        "display" : "Alazami-Yuan syndrome"
      },
      {
        "code" : "694956",
        "display" : "Intellectual disability-lymphoid hypertrophy-macrocephaly syndrome"
      },
      {
        "code" : "694963",
        "display" : "Inflammatory breast cancer"
      },
      {
        "code" : "695020",
        "display" : "Urachal carcinoma"
      },
      {
        "code" : "695023",
        "display" : "Pure squamous carcinoma of the urothelial tract"
      },
      {
        "code" : "695032",
        "display" : "Giant omphalocele"
      },
      {
        "code" : "695038",
        "display" : "Small omphalocele"
      },
      {
        "code" : "695110",
        "display" : "MAN2B2-CDG"
      },
      {
        "code" : "695131",
        "display" : "Acinar cystic transformation of the pancreas"
      },
      {
        "code" : "695136",
        "display" : "Infant-type hemispheric glioma"
      },
      {
        "code" : "695140",
        "display" : "Sickle cell-beta zero-thalassemia"
      },
      {
        "code" : "695147",
        "display" : "Sickle cell-beta plus-thalassemia"
      },
      {
        "code" : "695172",
        "display" : "Combined immunodeficiency due to dimerization defective IKAROS mutation"
      },
      {
        "code" : "695183",
        "display" : "Late-onset combined immunodeficiency due to ICOS deficiency"
      },
      {
        "code" : "695191",
        "display" : "Late-onset combined immunodeficiency due to ICOSL deficiency"
      },
      {
        "code" : "695611",
        "display" : "3q26q28 deletion syndrome"
      },
      {
        "code" : "695631",
        "display" : "Primary vitreoretinal large B-cell lymphoma"
      },
      {
        "code" : "695783",
        "display" : "EDEM3-CDG"
      },
      {
        "code" : "695807",
        "display" : "Immunodeficiency-systemic inflammation-lymphoma predisposition syndrome"
      },
      {
        "code" : "696063",
        "display" : "PLIN4-related distal myopathy"
      },
      {
        "code" : "696078",
        "display" : "Central Giant Cell Granuloma"
      },
      {
        "code" : "696175",
        "display" : "Encapsulating peritoneal sclerosis"
      },
      {
        "code" : "696189",
        "display" : "Congenital generalized lipodystrophy type 1"
      },
      {
        "code" : "696206",
        "display" : "Congenital generalized lipodystrophy type 3"
      },
      {
        "code" : "696242",
        "display" : "PPARG-associated congenital generalized lipodystrophy"
      },
      {
        "code" : "696289",
        "display" : "Congenital generalized lipodystrophy type 2"
      },
      {
        "code" : "69663",
        "display" : "Low phospholipid-associated cholelithiasis"
      },
      {
        "code" : "69665",
        "display" : "Intrahepatic cholestasis of pregnancy"
      },
      {
        "code" : "696830",
        "display" : "Female adnexal tumor of probable Wolffian origin"
      },
      {
        "code" : "696857",
        "display" : "Common variable immunodeficiency phenotype due to germinal digenic/polygenic mutations"
      },
      {
        "code" : "696863",
        "display" : "Common variable immunodeficiency phenotype due to somatic mutations"
      },
      {
        "code" : "696874",
        "display" : "NFKB1-related immune dysregulation"
      },
      {
        "code" : "696881",
        "display" : "Common variable immunodeficiency phenotype due to CD19/CD81 deficiency"
      },
      {
        "code" : "696894",
        "display" : "Common variable immunodeficiency phenotype due to CD21 deficiency"
      },
      {
        "code" : "696897",
        "display" : "Congenital megaprepuce"
      },
      {
        "code" : "696904",
        "display" : "Common variable immunodeficiency phenotype due to IRF2BP2 deficiency"
      },
      {
        "code" : "696907",
        "display" : "Common variable immunodeficiency phenotype due to homozygous TACI deficiency"
      },
      {
        "code" : "696925",
        "display" : "Adult-onset common variable immunodeficiency due to BAFF-receptor deficiency"
      },
      {
        "code" : "696931",
        "display" : "Common variable immunodeficiency phenotype due to TWEAK deficiency"
      },
      {
        "code" : "696942",
        "display" : "Childhood-onset common variable immunodeficiency due to ARHGEF1 deficiency"
      },
      {
        "code" : "696945",
        "display" : "X-linked common variable immunodeficiency phenotype due to SH3KBP1 deficiency"
      },
      {
        "code" : "697053",
        "display" : "Talaromycosis"
      },
      {
        "code" : "697067",
        "display" : "Global developmental delay-intellectual disability-microcephaly-short stature-brain iron accumulation syndrome"
      },
      {
        "code" : "697091",
        "display" : "Emergomycosis"
      },
      {
        "code" : "697096",
        "display" : "Cryptosporidiosis"
      },
      {
        "code" : "697101",
        "display" : "Fontaine progeroid syndrome"
      },
      {
        "code" : "697132",
        "display" : "Lymphoepithelial cyst of the pancreas"
      },
      {
        "code" : "697160",
        "display" : "Infantile epileptic spasms syndrome"
      },
      {
        "code" : "69723",
        "display" : "Tyrosinemia type 3"
      },
      {
        "code" : "69735",
        "display" : "Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome"
      },
      {
        "code" : "697356",
        "display" : "Congenital scalp aplasia cutis-enamel hypoplasia-developmental delay-intellectual disability syndrome"
      },
      {
        "code" : "69736",
        "display" : "Bilateral acute depigmentation of the iris"
      },
      {
        "code" : "69737",
        "display" : "Bosley-Salih-Alorainy syndrome"
      },
      {
        "code" : "697385",
        "display" : "Combined immunodeficiency-cancer predisposing syndrome due to AIOLOS deficiency"
      },
      {
        "code" : "697389",
        "display" : "Combined immunodeficiency due to HELIOS deficiency"
      },
      {
        "code" : "69739",
        "display" : "Athabaskan brainstem dysgenesis syndrome"
      },
      {
        "code" : "697394",
        "display" : "Combined immunodeficiency due to c-REL deficiency"
      },
      {
        "code" : "697403",
        "display" : "Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to IKBKA deficiency"
      },
      {
        "code" : "697414",
        "display" : "Early-onset combined immunodeficiency with low Ig due to dominant negative IKAROS mutation"
      },
      {
        "code" : "697417",
        "display" : "Common variable immunodeficiency phenotype due to SEC61A1 deficiency"
      },
      {
        "code" : "69744",
        "display" : "Circumscribed palmoplantar hypokeratosis"
      },
      {
        "code" : "69745",
        "display" : "Warty dyskeratoma"
      },
      {
        "code" : "697734",
        "display" : "ST3GAL3-CDG"
      },
      {
        "code" : "697760",
        "display" : "Intellectual disability-nasal speech-craniofacial dysmorphism syndrome"
      },
      {
        "code" : "697764",
        "display" : "Intellectual disability-nasal speech-craniofacial dysmorphism syndrome due to CNOT2 mutation"
      },
      {
        "code" : "697986",
        "display" : "Congenital peritoneal encapsulation"
      },
      {
        "code" : "698005",
        "display" : "Epilepsy with generalized tonic-clonic seizures alone"
      },
      {
        "code" : "698012",
        "display" : "Fibromuscular dysplasia"
      },
      {
        "code" : "698036",
        "display" : "Fibromuscular dysplasia of the cervical and intracranial arteries"
      },
      {
        "code" : "698043",
        "display" : "Fibromuscular dysplasia of the renal arteries"
      },
      {
        "code" : "698059",
        "display" : "Fibromuscular dysplasia of the coronary arteries"
      },
      {
        "code" : "698063",
        "display" : "Fibromuscular dysplasia of the visceral arteries"
      },
      {
        "code" : "698069",
        "display" : "Fibromuscular dysplasia of the arteries of the extremities"
      },
      {
        "code" : "698085",
        "display" : "Global developmental delay-intellectual disability-facial dysmorphism-pseudo-Pelger-Huët anomaly syndrome"
      },
      {
        "code" : "698090",
        "display" : "Ophthalmological abnormalities-facial dysmorphism-intellectual disability syndrome"
      },
      {
        "code" : "698260",
        "display" : "Carotid web"
      },
      {
        "code" : "698945",
        "display" : "Autoimmune heparin-induced thrombocytopenia"
      },
      {
        "code" : "699",
        "display" : "Pearson syndrome"
      },
      {
        "code" : "699021",
        "display" : "Spontaneous heparin-induced thrombocytopenia"
      },
      {
        "code" : "699029",
        "display" : "Vaccine-induced immune thrombotic thrombocytopenia"
      },
      {
        "code" : "699057",
        "display" : "Annular erythema of infancy"
      },
      {
        "code" : "699068",
        "display" : "Fontan-associated liver disease"
      },
      {
        "code" : "699578",
        "display" : "Combined immunodeficiency with low Ig due to BCL10 deficiency"
      },
      {
        "code" : "699590",
        "display" : "Immune dysregulation with immunodeficiency due to AIOLOS haploinsufficiency"
      },
      {
        "code" : "699593",
        "display" : "Combined immunodeficiency-lymphopenia-cancer predisposing syndrome due to AIOLOS deficiency"
      },
      {
        "code" : "699596",
        "display" : "Combined immunodeficiency-hypogammaglobulinemia-cancer predisposing syndrome due to AIOLOS deficiency"
      },
      {
        "code" : "699599",
        "display" : "ICHAD syndrome"
      },
      {
        "code" : "699605",
        "display" : "NEMO deleted exon 5 autoinflammatory syndrome"
      },
      {
        "code" : "699615",
        "display" : "Severe mendelian susceptibility to mycobacterial diseases due to complete IRF1 deficiency"
      },
      {
        "code" : "699618",
        "display" : "Severe mendelian susceptibility to mycobacterial diseases due to complete IFNG deficiency"
      },
      {
        "code" : "699678",
        "display" : "Necrotizing cellulitis"
      },
      {
        "code" : "699683",
        "display" : "Fibro-adipose vascular anomaly"
      },
      {
        "code" : "699697",
        "display" : "Necrotizing fasciitis"
      },
      {
        "code" : "699702",
        "display" : "Necrotizing myositis"
      },
      {
        "code" : "699708",
        "display" : "CLN14 disease"
      },
      {
        "code" : "699718",
        "display" : "Infantile CLN1 disease"
      },
      {
        "code" : "699734",
        "display" : "Late infantile CLN1 disease"
      },
      {
        "code" : "699739",
        "display" : "Juvenile CLN1 disease"
      },
      {
        "code" : "699745",
        "display" : "Adult CLN1 disease"
      },
      {
        "code" : "699751",
        "display" : "Infantile CLN2 disease"
      },
      {
        "code" : "699761",
        "display" : "Late infantile CLN2 disease"
      },
      {
        "code" : "699769",
        "display" : "Juvenile CLN2 disease"
      },
      {
        "code" : "699780",
        "display" : "Juvenile CLN3 disease"
      },
      {
        "code" : "699796",
        "display" : "Protracted juvenile CLN3 disease"
      },
      {
        "code" : "699802",
        "display" : "Late infantile CLN5 disease"
      },
      {
        "code" : "699807",
        "display" : "Juvenile CLN5 disease"
      },
      {
        "code" : "699812",
        "display" : "Adult CLN5 disease"
      },
      {
        "code" : "699822",
        "display" : "Sickle cell S-Lepore disease"
      },
      {
        "code" : "699835",
        "display" : "Cataract-combined malonic and methylmalonic aciduria-intellectual disability syndrome"
      },
      {
        "code" : "699844",
        "display" : "Microcephaly-corpus callosum hypoplasia-simplified gyral pattern-intellectual disability syndrome"
      },
      {
        "code" : "699850",
        "display" : "2p25.3 microduplication syndrome"
      },
      {
        "code" : "7",
        "display" : "3C syndrome"
      },
      {
        "code" : "70",
        "display" : "Proximal spinal muscular atrophy"
      },
      {
        "code" : "700",
        "display" : "Alopecia totalis"
      },
      {
        "code" : "700085",
        "display" : "Sickle cell disease due to hemoglobin S and a non-S/non-C hemoglobin variant"
      },
      {
        "code" : "700090",
        "display" : "Sickle cell S-O Arab disease"
      },
      {
        "code" : "700107",
        "display" : "Sickle cell S-other specified hemoglobin variant"
      },
      {
        "code" : "700111",
        "display" : "Homozygous hemoglobin O Arab disease"
      },
      {
        "code" : "700124",
        "display" : "Autosomal recessive hereditary chronic pancreatitis"
      },
      {
        "code" : "700133",
        "display" : "Idiopathic chronic pancreatitis"
      },
      {
        "code" : "700136",
        "display" : "Early-onset idiopathic chronic pancreatitis"
      },
      {
        "code" : "700139",
        "display" : "Late-onset idiopathic chronic pancreatitis"
      },
      {
        "code" : "700154",
        "display" : "TARDBP-related predominantly upper-limb distal myopathy"
      },
      {
        "code" : "700160",
        "display" : "ADNP-related blepharophimosis-intellectual disability syndrome"
      },
      {
        "code" : "700163",
        "display" : "SMPX-related distal myopathy"
      },
      {
        "code" : "700170",
        "display" : "Asymetric thumb-handgrip weakness-distal myopathy"
      },
      {
        "code" : "700188",
        "display" : "Calf-predominant weakness-gastrocnemius medialis atrophy-distal myopathy"
      },
      {
        "code" : "700205",
        "display" : "Combined immunodeficiency due to IKBKB gain-of-function mutation"
      },
      {
        "code" : "700286",
        "display" : "Congenital high airway obstruction syndrome"
      },
      {
        "code" : "700325",
        "display" : "NKAP-related intellectual disability-facial dysmorphism-marfanoid habitus-scoliosis syndrome"
      },
      {
        "code" : "700333",
        "display" : "Hypotonia-speech impairment-severe cognitive delay syndrome due to UNC80 deficiency"
      },
      {
        "code" : "700336",
        "display" : "Hypotonia-speech impairment-severe cognitive delay syndrome due to NALCN deficiency"
      },
      {
        "code" : "700467",
        "display" : "Late infantile CLN6 disease"
      },
      {
        "code" : "700472",
        "display" : "Juvenile CLN6 disease"
      },
      {
        "code" : "700477",
        "display" : "Adult CLN6 disease"
      },
      {
        "code" : "700484",
        "display" : "Late infantile CLN8 disease"
      },
      {
        "code" : "700487",
        "display" : "Congenital CLN10 disease"
      },
      {
        "code" : "700492",
        "display" : "Late infantile CLN10 disease"
      },
      {
        "code" : "700497",
        "display" : "Juvenile CLN10 disease"
      },
      {
        "code" : "700508",
        "display" : "Distal muscle weakness-foot deformity-elevated sorbitol level-hereditary motor neuropathy"
      },
      {
        "code" : "701",
        "display" : "Alopecia universalis"
      },
      {
        "code" : "702",
        "display" : "Pelizaeus-Merzbacher disease"
      },
      {
        "code" : "703",
        "display" : "Bullous pemphigoid"
      },
      {
        "code" : "704",
        "display" : "Pemphigus vulgaris"
      },
      {
        "code" : "70472",
        "display" : "Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type"
      },
      {
        "code" : "70475",
        "display" : "Radiation proctitis"
      },
      {
        "code" : "70476",
        "display" : "Vernal keratoconjunctivitis"
      },
      {
        "code" : "705",
        "display" : "Pendred syndrome"
      },
      {
        "code" : "70567",
        "display" : "Cholangiocarcinoma"
      },
      {
        "code" : "70568",
        "display" : "Post-transplant lymphoproliferative disease"
      },
      {
        "code" : "70573",
        "display" : "Small cell lung cancer"
      },
      {
        "code" : "70578",
        "display" : "Adult acute respiratory distress syndrome"
      },
      {
        "code" : "70588",
        "display" : "Meconium aspiration syndrome"
      },
      {
        "code" : "70589",
        "display" : "Bronchopulmonary dysplasia"
      },
      {
        "code" : "70590",
        "display" : "Infantile apnea"
      },
      {
        "code" : "70591",
        "display" : "Chronic thromboembolic pulmonary hypertension"
      },
      {
        "code" : "70592",
        "display" : "Transient predisposition to invasive pyogenic bacterial infection"
      },
      {
        "code" : "70593",
        "display" : "Immunodeficiency due to selective anti-polysaccharide antibody deficiency"
      },
      {
        "code" : "70594",
        "display" : "Dopa-responsive dystonia due to sepiapterin reductase deficiency"
      },
      {
        "code" : "70595",
        "display" : "Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome"
      },
      {
        "code" : "70596",
        "display" : "Congenital Epstein-Barr virus infection"
      },
      {
        "code" : "707",
        "display" : "Plague"
      },
      {
        "code" : "708",
        "display" : "Peters anomaly"
      },
      {
        "code" : "709",
        "display" : "Peters plus syndrome"
      },
      {
        "code" : "71",
        "display" : "Chylomicron retention disease"
      },
      {
        "code" : "710",
        "display" : "Pfeiffer syndrome"
      },
      {
        "code" : "712",
        "display" : "Hemolytic anemia due to glucophosphate isomerase deficiency"
      },
      {
        "code" : "71211",
        "display" : "Neuromyelitis optica spectrum disorder"
      },
      {
        "code" : "71212",
        "display" : "Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency"
      },
      {
        "code" : "71213",
        "display" : "Retinal capillary malformation"
      },
      {
        "code" : "71267",
        "display" : "Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome"
      },
      {
        "code" : "71271",
        "display" : "Split hand-split foot-deafness syndrome"
      },
      {
        "code" : "71272",
        "display" : "Sandifer syndrome"
      },
      {
        "code" : "71273",
        "display" : "Renal nutcracker syndrome"
      },
      {
        "code" : "71274",
        "display" : "Disseminated peritoneal leiomyomatosis"
      },
      {
        "code" : "71275",
        "display" : "Rh deficiency syndrome"
      },
      {
        "code" : "71276",
        "display" : "Silent sinus syndrome"
      },
      {
        "code" : "71277",
        "display" : "Classic glucose transporter type 1 deficiency syndrome"
      },
      {
        "code" : "71278",
        "display" : "Congenital brain dysgenesis due to glutamine synthetase deficiency"
      },
      {
        "code" : "71279",
        "display" : "CANOMAD syndrome"
      },
      {
        "code" : "71289",
        "display" : "Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome"
      },
      {
        "code" : "71290",
        "display" : "Familial platelet disorder with associated myeloid malignancy"
      },
      {
        "code" : "713",
        "display" : "Glycogen storage disease due to phosphoglycerate kinase 1 deficiency"
      },
      {
        "code" : "714",
        "display" : "Hemolytic anemia due to diphosphoglycerate mutase deficiency"
      },
      {
        "code" : "71493",
        "display" : "Familial thrombocytosis"
      },
      {
        "code" : "715",
        "display" : "Glycogen storage disease due to muscle phosphorylase kinase deficiency"
      },
      {
        "code" : "71505",
        "display" : "Cancer-associated retinopathy"
      },
      {
        "code" : "71517",
        "display" : "Rapid-onset dystonia-parkinsonism"
      },
      {
        "code" : "71518",
        "display" : "Benign paroxysmal torticollis of infancy"
      },
      {
        "code" : "71519",
        "display" : "Psychogenic movement disorders"
      },
      {
        "code" : "71526",
        "display" : "Obesity due to pro-opiomelanocortin deficiency"
      },
      {
        "code" : "71528",
        "display" : "Obesity due to prohormone convertase I deficiency"
      },
      {
        "code" : "71529",
        "display" : "Obesity due to melanocortin 4 receptor deficiency"
      },
      {
        "code" : "716",
        "display" : "Phenylketonuria"
      },
      {
        "code" : "718",
        "display" : "Isolated Pierre Robin sequence"
      },
      {
        "code" : "72",
        "display" : "Angelman syndrome"
      },
      {
        "code" : "720",
        "display" : "Pili bifurcati"
      },
      {
        "code" : "721",
        "display" : "Gray platelet syndrome"
      },
      {
        "code" : "722",
        "display" : "Hypoplasminogenemia"
      },
      {
        "code" : "723",
        "display" : "Pneumocystosis"
      },
      {
        "code" : "724",
        "display" : "Idiopathic acute eosinophilic pneumonia"
      },
      {
        "code" : "725",
        "display" : "Developmental and epileptic encephalopathy with spike-wave activation in sleep"
      },
      {
        "code" : "726",
        "display" : "Alpers-Huttenlocher syndrome"
      },
      {
        "code" : "727",
        "display" : "Microscopic polyangiitis"
      },
      {
        "code" : "728",
        "display" : "Relapsing polychondritis"
      },
      {
        "code" : "729",
        "display" : "Polycythemia vera"
      },
      {
        "code" : "73",
        "display" : "Gorham-Stout disease"
      },
      {
        "code" : "730",
        "display" : "Autosomal dominant polycystic kidney disease"
      },
      {
        "code" : "731",
        "display" : "Autosomal recessive polycystic kidney disease"
      },
      {
        "code" : "732",
        "display" : "Polymyositis"
      },
      {
        "code" : "73223",
        "display" : "Global developmental delay-osteopenia-ectodermal defect syndrome"
      },
      {
        "code" : "73224",
        "display" : "Kidney tubulopathy-dilated cardiomyopathy syndrome"
      },
      {
        "code" : "73229",
        "display" : "HANAC syndrome"
      },
      {
        "code" : "73230",
        "display" : "Ossification anomalies-psychomotor developmental delay syndrome"
      },
      {
        "code" : "73245",
        "display" : "Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome"
      },
      {
        "code" : "73246",
        "display" : "Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome"
      },
      {
        "code" : "73256",
        "display" : "Central neurocytoma"
      },
      {
        "code" : "73260",
        "display" : "Paracoccidioidomycosis"
      },
      {
        "code" : "73263",
        "display" : "Zygomycosis"
      },
      {
        "code" : "73267",
        "display" : "Non-24-hour sleep-wake syndrome"
      },
      {
        "code" : "73271",
        "display" : "Bleeding diathesis due to a collagen receptor defect"
      },
      {
        "code" : "73272",
        "display" : "Growth delay due to insulin-like growth factor type 1 deficiency"
      },
      {
        "code" : "73273",
        "display" : "Growth delay due to insulin-like growth factor I resistance"
      },
      {
        "code" : "733",
        "display" : "Familial adenomatous polyposis"
      },
      {
        "code" : "734",
        "display" : "Alpha delta granule deficiency"
      },
      {
        "code" : "73423",
        "display" : "Acute ackee fruit intoxication"
      },
      {
        "code" : "735",
        "display" : "Porokeratosis of Mibelli"
      },
      {
        "code" : "737",
        "display" : "Porokeratosis plantaris palmaris et disseminata"
      },
      {
        "code" : "739",
        "display" : "Prader-Willi syndrome"
      },
      {
        "code" : "74",
        "display" : "Angiostrongyliasis"
      },
      {
        "code" : "740",
        "display" : "Hutchinson-Gilford progeria syndrome"
      },
      {
        "code" : "741",
        "display" : "Familial mitral valve prolapse"
      },
      {
        "code" : "742",
        "display" : "Prolidase deficiency"
      },
      {
        "code" : "743",
        "display" : "Severe hereditary thrombophilia due to congenital protein S deficiency"
      },
      {
        "code" : "744",
        "display" : "Proteus syndrome"
      },
      {
        "code" : "745",
        "display" : "Severe hereditary thrombophilia due to congenital protein C deficiency"
      },
      {
        "code" : "746",
        "display" : "Mitochondrial trifunctional protein deficiency"
      },
      {
        "code" : "747",
        "display" : "Autoimmune pulmonary alveolar proteinosis"
      },
      {
        "code" : "749",
        "display" : "Congenital prekallikrein deficiency"
      },
      {
        "code" : "750",
        "display" : "Pseudoachondroplasia"
      },
      {
        "code" : "752",
        "display" : "46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency"
      },
      {
        "code" : "75233",
        "display" : "Wolman disease"
      },
      {
        "code" : "75234",
        "display" : "Cholesteryl ester storage disease"
      },
      {
        "code" : "75249",
        "display" : "Familial isolated restrictive cardiomyopathy"
      },
      {
        "code" : "753",
        "display" : "46,XY difference of sex development due to 5-alpha-reductase 2 deficiency"
      },
      {
        "code" : "75325",
        "display" : "Osteosclerosis-ichthyosis-premature ovarian failure syndrome"
      },
      {
        "code" : "75326",
        "display" : "Familial isolated retinal arteriolar tortuosity"
      },
      {
        "code" : "75327",
        "display" : "North Carolina macular dystrophy"
      },
      {
        "code" : "75373",
        "display" : "Progressive bifocal chorioretinal atrophy"
      },
      {
        "code" : "75374",
        "display" : "Bradyopsia"
      },
      {
        "code" : "75376",
        "display" : "Familial drusen"
      },
      {
        "code" : "75377",
        "display" : "Central areolar choroidal dystrophy"
      },
      {
        "code" : "75378",
        "display" : "Oligocone trichromacy"
      },
      {
        "code" : "75381",
        "display" : "Cystoid macular dystrophy"
      },
      {
        "code" : "75382",
        "display" : "Oguchi disease"
      },
      {
        "code" : "75389",
        "display" : "Brain malformation-congenital heart disease-postaxial polydactyly syndrome"
      },
      {
        "code" : "75391",
        "display" : "Primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency"
      },
      {
        "code" : "75392",
        "display" : "Periodontal Ehlers-Danlos syndrome"
      },
      {
        "code" : "75496",
        "display" : "B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome"
      },
      {
        "code" : "75497",
        "display" : "X-linked Ehlers-Danlos syndrome"
      },
      {
        "code" : "755",
        "display" : "Leydig cell hypoplasia"
      },
      {
        "code" : "75508",
        "display" : "Angioosteohypotrophic syndrome"
      },
      {
        "code" : "75563",
        "display" : "X-linked sideroblastic anemia"
      },
      {
        "code" : "75564",
        "display" : "Acquired idiopathic sideroblastic anemia"
      },
      {
        "code" : "75565",
        "display" : "Tropical endomyocardial fibrosis"
      },
      {
        "code" : "75566",
        "display" : "Loeffler endocarditis"
      },
      {
        "code" : "75567",
        "display" : "Primary progressive freezing gait"
      },
      {
        "code" : "756",
        "display" : "Pseudohypoaldosteronism type 1"
      },
      {
        "code" : "757",
        "display" : "Pseudohypoaldosteronism type 2"
      },
      {
        "code" : "758",
        "display" : "Pseudoxanthoma elasticum"
      },
      {
        "code" : "75840",
        "display" : "Ullrich congenital muscular dystrophy"
      },
      {
        "code" : "75857",
        "display" : "6q terminal deletion syndrome"
      },
      {
        "code" : "75858",
        "display" : "MORM syndrome"
      },
      {
        "code" : "76",
        "display" : "Strongyloidiasis"
      },
      {
        "code" : "760",
        "display" : "Purine nucleoside phosphorylase deficiency"
      },
      {
        "code" : "761",
        "display" : "Immunoglobulin A vasculitis"
      },
      {
        "code" : "763",
        "display" : "Pycnodysostosis"
      },
      {
        "code" : "764",
        "display" : "Pyomyositis"
      },
      {
        "code" : "765",
        "display" : "Pyruvate dehydrogenase deficiency"
      },
      {
        "code" : "766",
        "display" : "Hemolytic anemia due to red cell pyruvate kinase deficiency"
      },
      {
        "code" : "767",
        "display" : "Polyarteritis nodosa"
      },
      {
        "code" : "769",
        "display" : "Rabson-Mendenhall syndrome"
      },
      {
        "code" : "770",
        "display" : "Rabies"
      },
      {
        "code" : "772",
        "display" : "Infantile Refsum disease"
      },
      {
        "code" : "77258",
        "display" : "Trichorhinophalangeal syndrome type 1"
      },
      {
        "code" : "77259",
        "display" : "Gaucher disease type 1"
      },
      {
        "code" : "77260",
        "display" : "Gaucher disease type 2"
      },
      {
        "code" : "77261",
        "display" : "Gaucher disease type 3"
      },
      {
        "code" : "77292",
        "display" : "Infantile neurovisceral acid sphingomyelinase deficiency"
      },
      {
        "code" : "77293",
        "display" : "Chronic visceral acid sphingomyelinase deficiency"
      },
      {
        "code" : "77295",
        "display" : "Odontoleukodystrophy"
      },
      {
        "code" : "77296",
        "display" : "Morgagni-Stewart-Morel syndrome"
      },
      {
        "code" : "77297",
        "display" : "Majeed syndrome"
      },
      {
        "code" : "77298",
        "display" : "Anophthalmia/microphthalmia-esophageal atresia syndrome"
      },
      {
        "code" : "77299",
        "display" : "Microphthalmia-brain atrophy syndrome"
      },
      {
        "code" : "773",
        "display" : "Refsum disease"
      },
      {
        "code" : "77300",
        "display" : "Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome"
      },
      {
        "code" : "77301",
        "display" : "Monosomy 9q22.3 syndrome"
      },
      {
        "code" : "774",
        "display" : "Hereditary hemorrhagic telangiectasia"
      },
      {
        "code" : "776",
        "display" : "Lujan-Fryns syndrome"
      },
      {
        "code" : "777",
        "display" : "X-linked non-syndromic intellectual disability"
      },
      {
        "code" : "778",
        "display" : "Rett syndrome"
      },
      {
        "code" : "779",
        "display" : "Reynolds syndrome"
      },
      {
        "code" : "78",
        "display" : "Ankylostomiasis"
      },
      {
        "code" : "780",
        "display" : "Rhabdomyosarcoma"
      },
      {
        "code" : "781",
        "display" : "Q fever"
      },
      {
        "code" : "782",
        "display" : "Axenfeld-Rieger syndrome"
      },
      {
        "code" : "783",
        "display" : "Rubinstein-Taybi syndrome"
      },
      {
        "code" : "785",
        "display" : "Estrogen resistance syndrome"
      },
      {
        "code" : "786",
        "display" : "Generalized glucocorticoid resistance syndrome"
      },
      {
        "code" : "79",
        "display" : "Congenital alpha2-antiplasmin deficiency"
      },
      {
        "code" : "790",
        "display" : "Retinoblastoma"
      },
      {
        "code" : "79076",
        "display" : "Juvenile polyposis of infancy"
      },
      {
        "code" : "79078",
        "display" : "IgG4-related dacryoadenitis and sialadenitis"
      },
      {
        "code" : "79083",
        "display" : "PPARG-related familial partial lipodystrophy"
      },
      {
        "code" : "79084",
        "display" : "Familial partial lipodystrophy, Köbberling type"
      },
      {
        "code" : "79085",
        "display" : "AKT2-related familial partial lipodystrophy"
      },
      {
        "code" : "79086",
        "display" : "Acquired generalized lipodystrophy"
      },
      {
        "code" : "79087",
        "display" : "Acquired partial lipodystrophy"
      },
      {
        "code" : "79091",
        "display" : "Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome"
      },
      {
        "code" : "79093",
        "display" : "Foix-Alajouanine syndrome"
      },
      {
        "code" : "79094",
        "display" : "Grange syndrome"
      },
      {
        "code" : "79095",
        "display" : "Congenital bile acid synthesis defect type 4"
      },
      {
        "code" : "79096",
        "display" : "Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy"
      },
      {
        "code" : "79097",
        "display" : "Folinic acid-responsive seizures"
      },
      {
        "code" : "79098",
        "display" : "Sympathetic ophthalmia"
      },
      {
        "code" : "79099",
        "display" : "Interstitial granulomatous dermatitis with arthritis"
      },
      {
        "code" : "791",
        "display" : "Retinitis pigmentosa"
      },
      {
        "code" : "79100",
        "display" : "Atrophoderma vermiculata"
      },
      {
        "code" : "79101",
        "display" : "Hyperprolinemia type 2"
      },
      {
        "code" : "79102",
        "display" : "Thyrotoxic periodic paralysis"
      },
      {
        "code" : "79105",
        "display" : "Myxofibrosarcoma"
      },
      {
        "code" : "79106",
        "display" : "Eiken syndrome"
      },
      {
        "code" : "79107",
        "display" : "Developmental malformations-deafness-dystonia syndrome"
      },
      {
        "code" : "79113",
        "display" : "Mandibulofacial dysostosis-microcephaly syndrome"
      },
      {
        "code" : "79118",
        "display" : "Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome"
      },
      {
        "code" : "79124",
        "display" : "Hepatic veno-occlusive disease-immunodeficiency syndrome"
      },
      {
        "code" : "79126",
        "display" : "Acute interstitial pneumonia"
      },
      {
        "code" : "79127",
        "display" : "Respiratory bronchiolitis-interstitial lung disease syndrome"
      },
      {
        "code" : "79128",
        "display" : "Lymphoid interstitial pneumonia"
      },
      {
        "code" : "79129",
        "display" : "Trichodysplasia-amelogenesis imperfecta syndrome"
      },
      {
        "code" : "79133",
        "display" : "Focal facial dermal dysplasia type I"
      },
      {
        "code" : "79134",
        "display" : "DEND syndrome"
      },
      {
        "code" : "79135",
        "display" : "Episodic ataxia type 3"
      },
      {
        "code" : "79136",
        "display" : "Episodic ataxia type 4"
      },
      {
        "code" : "79137",
        "display" : "Generalized epilepsy-paroxysmal dyskinesia syndrome"
      },
      {
        "code" : "79138",
        "display" : "Bickerstaff brainstem encephalitis"
      },
      {
        "code" : "79139",
        "display" : "Japanese encephalitis"
      },
      {
        "code" : "79140",
        "display" : "Cutaneous neuroendocrine carcinoma"
      },
      {
        "code" : "79141",
        "display" : "Hereditary painful callosities"
      },
      {
        "code" : "79143",
        "display" : "Isolated congenital anonychia"
      },
      {
        "code" : "79144",
        "display" : "Isolated congenital onychodysplasia"
      },
      {
        "code" : "79145",
        "display" : "Dowling-Degos disease"
      },
      {
        "code" : "79146",
        "display" : "Familial progressive hyperpigmentation"
      },
      {
        "code" : "79147",
        "display" : "Familial reactive perforating collagenosis"
      },
      {
        "code" : "79148",
        "display" : "Elastosis perforans serpiginosa"
      },
      {
        "code" : "79149",
        "display" : "Dermochondrocorneal dystrophy"
      },
      {
        "code" : "79150",
        "display" : "Linear and whorled nevoid hypermelanosis"
      },
      {
        "code" : "79151",
        "display" : "Acrokeratosis verruciformis of Hopf"
      },
      {
        "code" : "79152",
        "display" : "Disseminated superficial actinic porokeratosis"
      },
      {
        "code" : "79153",
        "display" : "Idiopathic trachyonychia"
      },
      {
        "code" : "79154",
        "display" : "2-aminoadipic 2-oxoadipic aciduria"
      },
      {
        "code" : "79155",
        "display" : "Hydroxykynureninuria"
      },
      {
        "code" : "79156",
        "display" : "Seizures-intellectual disability due to hydroxylysinuria syndrome"
      },
      {
        "code" : "79157",
        "display" : "2-methylbutyryl-CoA dehydrogenase deficiency"
      },
      {
        "code" : "79159",
        "display" : "Isobutyryl-CoA dehydrogenase deficiency"
      },
      {
        "code" : "792",
        "display" : "X-linked retinoschisis"
      },
      {
        "code" : "79230",
        "display" : "HJV or HAMP-related hemochromatosis"
      },
      {
        "code" : "79233",
        "display" : "Hypoxanthine guanine phosphoribosyltransferase partial deficiency"
      },
      {
        "code" : "79234",
        "display" : "Crigler-Najjar syndrome type 1"
      },
      {
        "code" : "79235",
        "display" : "Crigler-Najjar syndrome type 2"
      },
      {
        "code" : "79237",
        "display" : "Galactokinase deficiency"
      },
      {
        "code" : "79238",
        "display" : "Galactose epimerase deficiency"
      },
      {
        "code" : "79239",
        "display" : "Classic galactosemia"
      },
      {
        "code" : "79240",
        "display" : "Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency"
      },
      {
        "code" : "79241",
        "display" : "Biotinidase deficiency"
      },
      {
        "code" : "79242",
        "display" : "Holocarboxylase synthetase deficiency"
      },
      {
        "code" : "79243",
        "display" : "Pyruvate dehydrogenase E1-alpha deficiency"
      },
      {
        "code" : "79244",
        "display" : "Pyruvate dehydrogenase E2 deficiency"
      },
      {
        "code" : "79246",
        "display" : "Pyruvate dehydrogenase phosphatase deficiency"
      },
      {
        "code" : "79253",
        "display" : "Mild phenylketonuria"
      },
      {
        "code" : "79254",
        "display" : "Classic phenylketonuria"
      },
      {
        "code" : "79255",
        "display" : "GM1 gangliosidosis type 1"
      },
      {
        "code" : "79256",
        "display" : "GM1 gangliosidosis type 2"
      },
      {
        "code" : "79257",
        "display" : "GM1 gangliosidosis type 3"
      },
      {
        "code" : "79258",
        "display" : "Glycogen storage disease due to glucose-6-phosphatase deficiency type Ia"
      },
      {
        "code" : "79259",
        "display" : "Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib"
      },
      {
        "code" : "79269",
        "display" : "Sanfilippo syndrome type A"
      },
      {
        "code" : "79270",
        "display" : "Sanfilippo syndrome type B"
      },
      {
        "code" : "79271",
        "display" : "Sanfilippo syndrome type C"
      },
      {
        "code" : "79272",
        "display" : "Sanfilippo syndrome type D"
      },
      {
        "code" : "79273",
        "display" : "Hereditary coproporphyria"
      },
      {
        "code" : "79276",
        "display" : "Acute intermittent porphyria"
      },
      {
        "code" : "79277",
        "display" : "Congenital erythropoietic porphyria"
      },
      {
        "code" : "79278",
        "display" : "Autosomal erythropoietic protoporphyria"
      },
      {
        "code" : "79279",
        "display" : "Alpha-N-acetylgalactosaminidase deficiency type 1"
      },
      {
        "code" : "79280",
        "display" : "Alpha-N-acetylgalactosaminidase deficiency type 2"
      },
      {
        "code" : "79281",
        "display" : "Alpha-N-acetylgalactosaminidase deficiency type 3"
      },
      {
        "code" : "79282",
        "display" : "Methylmalonic acidemia with homocystinuria, type cblC"
      },
      {
        "code" : "79283",
        "display" : "Methylmalonic acidemia with homocystinuria, type cblD"
      },
      {
        "code" : "79284",
        "display" : "Methylmalonic acidemia with homocystinuria type cblF"
      },
      {
        "code" : "79292",
        "display" : "Fish-eye disease"
      },
      {
        "code" : "79293",
        "display" : "Familial LCAT deficiency"
      },
      {
        "code" : "79299",
        "display" : "Congenital glucokinase-related hyperinsulinism"
      },
      {
        "code" : "793",
        "display" : "SAPHO syndrome"
      },
      {
        "code" : "79301",
        "display" : "Congenital bile acid synthesis defect type 1"
      },
      {
        "code" : "79302",
        "display" : "Congenital bile acid synthesis defect type 3"
      },
      {
        "code" : "79303",
        "display" : "Congenital bile acid synthesis defect type 2"
      },
      {
        "code" : "79304",
        "display" : "Progressive familial intrahepatic cholestasis type 2"
      },
      {
        "code" : "79305",
        "display" : "Progressive familial intrahepatic cholestasis type 3"
      },
      {
        "code" : "79306",
        "display" : "Progressive familial intrahepatic cholestasis type 1"
      },
      {
        "code" : "79310",
        "display" : "Vitamin B12-responsive methylmalonic acidemia type cblA"
      },
      {
        "code" : "79311",
        "display" : "Vitamin B12-responsive methylmalonic acidemia type cblB"
      },
      {
        "code" : "79312",
        "display" : "Vitamin B12-unresponsive methylmalonic acidemia type mut-"
      },
      {
        "code" : "79314",
        "display" : "L-2-hydroxyglutaric aciduria"
      },
      {
        "code" : "79315",
        "display" : "D-2-hydroxyglutaric aciduria"
      },
      {
        "code" : "79318",
        "display" : "PMM2-CDG"
      },
      {
        "code" : "79319",
        "display" : "MPI-CDG"
      },
      {
        "code" : "79320",
        "display" : "ALG6-CDG"
      },
      {
        "code" : "79321",
        "display" : "ALG3-CDG"
      },
      {
        "code" : "79322",
        "display" : "DPM1-CDG"
      },
      {
        "code" : "79323",
        "display" : "MPDU1-CDG"
      },
      {
        "code" : "79324",
        "display" : "ALG12-CDG"
      },
      {
        "code" : "79325",
        "display" : "ALG8-CDG"
      },
      {
        "code" : "79326",
        "display" : "ALG2-CDG"
      },
      {
        "code" : "79327",
        "display" : "ALG1-CDG"
      },
      {
        "code" : "79328",
        "display" : "ALG9-CDG"
      },
      {
        "code" : "79329",
        "display" : "MGAT2-CDG"
      },
      {
        "code" : "79330",
        "display" : "MOGS-CDG"
      },
      {
        "code" : "79332",
        "display" : "B4GALT1-CDG"
      },
      {
        "code" : "79333",
        "display" : "COG7-CDG"
      },
      {
        "code" : "79345",
        "display" : "Brachytelephalangic chondrodysplasia punctata"
      },
      {
        "code" : "79346",
        "display" : "Chondrodysplasia punctata, tibial-metacarpal type"
      },
      {
        "code" : "79347",
        "display" : "Chondrodysplasia punctata, Toriello type"
      },
      {
        "code" : "79350",
        "display" : "3-phosphoserine phosphatase deficiency, infantile/juvenile form"
      },
      {
        "code" : "79351",
        "display" : "3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form"
      },
      {
        "code" : "79394",
        "display" : "Congenital ichthyosiform erythroderma"
      },
      {
        "code" : "79395",
        "display" : "Keratoderma hereditarium mutilans with ichthyosis"
      },
      {
        "code" : "79396",
        "display" : "Autosomal dominant generalized epidermolysis bullosa simplex, severe form"
      },
      {
        "code" : "79397",
        "display" : "Epidermolysis bullosa simplex with mottled pigmentation"
      },
      {
        "code" : "79399",
        "display" : "Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form"
      },
      {
        "code" : "794",
        "display" : "Saethre-Chotzen syndrome"
      },
      {
        "code" : "79400",
        "display" : "Localized epidermolysis bullosa simplex"
      },
      {
        "code" : "79401",
        "display" : "PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement"
      },
      {
        "code" : "79402",
        "display" : "Intermediate generalized junctional epidermolysis bullosa"
      },
      {
        "code" : "79403",
        "display" : "Junctional epidermolysis bullosa with pyloric atresia"
      },
      {
        "code" : "79404",
        "display" : "Severe generalized junctional epidermolysis bullosa"
      },
      {
        "code" : "79405",
        "display" : "Junctional epidermolysis bullosa inversa"
      },
      {
        "code" : "79406",
        "display" : "Late-onset junctional epidermolysis bullosa"
      },
      {
        "code" : "79408",
        "display" : "Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form"
      },
      {
        "code" : "79409",
        "display" : "Recessive dystrophic epidermolysis bullosa inversa"
      },
      {
        "code" : "79410",
        "display" : "Localized dystrophic epidermolysis bullosa, pretibial form"
      },
      {
        "code" : "79411",
        "display" : "Self-improving dystrophic epidermolysis bullosa"
      },
      {
        "code" : "79414",
        "display" : "Woolly hair nevus"
      },
      {
        "code" : "79430",
        "display" : "Hermansky-Pudlak syndrome"
      },
      {
        "code" : "79431",
        "display" : "Oculocutaneous albinism type 1A"
      },
      {
        "code" : "79432",
        "display" : "Oculocutaneous albinism type 2"
      },
      {
        "code" : "79433",
        "display" : "Oculocutaneous albinism type 3"
      },
      {
        "code" : "79434",
        "display" : "Oculocutaneous albinism type 1B"
      },
      {
        "code" : "79435",
        "display" : "Oculocutaneous albinism type 4"
      },
      {
        "code" : "79443",
        "display" : "Pseudohypoparathyroidism type 1A"
      },
      {
        "code" : "79444",
        "display" : "Pseudohypoparathyroidism type 1C"
      },
      {
        "code" : "79445",
        "display" : "Pseudopseudohypoparathyroidism"
      },
      {
        "code" : "79447",
        "display" : "X-linked lethal multiple pterygium syndrome"
      },
      {
        "code" : "79452",
        "display" : "Milroy disease"
      },
      {
        "code" : "79455",
        "display" : "Cutaneous mastocytoma"
      },
      {
        "code" : "79456",
        "display" : "Diffuse cutaneous mastocytosis"
      },
      {
        "code" : "79457",
        "display" : "Maculopapular cutaneous mastocytosis"
      },
      {
        "code" : "79466",
        "display" : "Inflammatory linear verrucous epidermal nevus"
      },
      {
        "code" : "79467",
        "display" : "Verrucous nevus"
      },
      {
        "code" : "79468",
        "display" : "Acanthokeratolytic verrucous nevus"
      },
      {
        "code" : "79473",
        "display" : "Variegate porphyria"
      },
      {
        "code" : "79474",
        "display" : "Atypical Werner syndrome"
      },
      {
        "code" : "79476",
        "display" : "Griscelli syndrome type 1"
      },
      {
        "code" : "79477",
        "display" : "Griscelli syndrome type 2"
      },
      {
        "code" : "79478",
        "display" : "Griscelli syndrome type 3"
      },
      {
        "code" : "79479",
        "display" : "Pemphigus vegetans"
      },
      {
        "code" : "79480",
        "display" : "Pemphigus erythematosus"
      },
      {
        "code" : "79481",
        "display" : "Pemphigus foliaceus"
      },
      {
        "code" : "79483",
        "display" : "Phakomatosis cesioflammea"
      },
      {
        "code" : "79484",
        "display" : "Phakomatosis cesiomarmorata"
      },
      {
        "code" : "79485",
        "display" : "Phakomatosis spilorosea"
      },
      {
        "code" : "79489",
        "display" : "Macrocystic lymphatic malformation"
      },
      {
        "code" : "79490",
        "display" : "Microcystic lymphatic malformation"
      },
      {
        "code" : "79492",
        "display" : "Pili gemini"
      },
      {
        "code" : "79493",
        "display" : "Brooke-Spiegler syndrome"
      },
      {
        "code" : "79495",
        "display" : "X-linked congenital generalized hypertrichosis"
      },
      {
        "code" : "79499",
        "display" : "Autosomal dominant deafness-onychodystrophy syndrome"
      },
      {
        "code" : "79500",
        "display" : "DOORS syndrome"
      },
      {
        "code" : "79501",
        "display" : "Punctate palmoplantar keratoderma type 1"
      },
      {
        "code" : "79502",
        "display" : "Punctate palmoplantar keratoderma type 2"
      },
      {
        "code" : "79503",
        "display" : "Ichthyosis hystrix of Curth-Macklin"
      },
      {
        "code" : "79507",
        "display" : "Hypotonia-failure to thrive-microcephaly syndrome"
      },
      {
        "code" : "796",
        "display" : "Sandhoff disease"
      },
      {
        "code" : "79643",
        "display" : "Autosomal recessive hyperinsulinism due to SUR1 deficiency"
      },
      {
        "code" : "79644",
        "display" : "Autosomal recessive hyperinsulinism due to Kir6.2 deficiency"
      },
      {
        "code" : "79651",
        "display" : "Mild hyperphenylalaninemia"
      },
      {
        "code" : "797",
        "display" : "Sarcoidosis"
      },
      {
        "code" : "798",
        "display" : "Schinzel-Giedion syndrome"
      },
      {
        "code" : "799",
        "display" : "Schizencephaly"
      },
      {
        "code" : "8",
        "display" : "47,XYY syndrome"
      },
      {
        "code" : "80",
        "display" : "Antiphospholipid syndrome"
      },
      {
        "code" : "800",
        "display" : "Schwartz-Jampel syndrome"
      },
      {
        "code" : "803",
        "display" : "Amyotrophic lateral sclerosis"
      },
      {
        "code" : "805",
        "display" : "Tuberous sclerosis complex"
      },
      {
        "code" : "806",
        "display" : "Scott syndrome"
      },
      {
        "code" : "808",
        "display" : "Seckel syndrome"
      },
      {
        "code" : "809",
        "display" : "Mixed connective tissue disease"
      },
      {
        "code" : "81",
        "display" : "Antisynthetase syndrome"
      },
      {
        "code" : "810",
        "display" : "Shigellosis"
      },
      {
        "code" : "811",
        "display" : "Shwachman-Diamond syndrome"
      },
      {
        "code" : "812",
        "display" : "Sialidosis type 1"
      },
      {
        "code" : "813",
        "display" : "Silver-Russell syndrome"
      },
      {
        "code" : "816",
        "display" : "Sjögren-Larsson syndrome"
      },
      {
        "code" : "818",
        "display" : "Smith-Lemli-Opitz syndrome"
      },
      {
        "code" : "819",
        "display" : "Smith-Magenis syndrome"
      },
      {
        "code" : "82",
        "display" : "Hereditary thrombophilia due to congenital antithrombin deficiency"
      },
      {
        "code" : "820",
        "display" : "Sneddon syndrome"
      },
      {
        "code" : "821",
        "display" : "Sotos syndrome"
      },
      {
        "code" : "822",
        "display" : "Hereditary spherocytosis"
      },
      {
        "code" : "824",
        "display" : "Primary myelofibrosis"
      },
      {
        "code" : "826",
        "display" : "Sporotrichosis"
      },
      {
        "code" : "827",
        "display" : "Stargardt disease"
      },
      {
        "code" : "828",
        "display" : "Stickler syndrome"
      },
      {
        "code" : "829",
        "display" : "Adult-onset Still disease"
      },
      {
        "code" : "83",
        "display" : "Antley-Bixler syndrome"
      },
      {
        "code" : "831",
        "display" : "Congenital cervical spinal stenosis"
      },
      {
        "code" : "832",
        "display" : "Succinyl-CoA:3-oxoacid CoA transferase deficiency"
      },
      {
        "code" : "833",
        "display" : "Encephalopathy due to sulfite oxidase deficiency"
      },
      {
        "code" : "83311",
        "display" : "Rocky Mountain spotted fever"
      },
      {
        "code" : "83312",
        "display" : "Rickettsialpox"
      },
      {
        "code" : "83313",
        "display" : "Boutonneuse fever"
      },
      {
        "code" : "83314",
        "display" : "Epidemic typhus"
      },
      {
        "code" : "83315",
        "display" : "Murine typhus"
      },
      {
        "code" : "83316",
        "display" : "Pseudotyphus of California"
      },
      {
        "code" : "83317",
        "display" : "Scrub typhus"
      },
      {
        "code" : "83330",
        "display" : "Proximal spinal muscular atrophy type 1"
      },
      {
        "code" : "834",
        "display" : "Free sialic acid storage disease"
      },
      {
        "code" : "83418",
        "display" : "Proximal spinal muscular atrophy type 2"
      },
      {
        "code" : "83419",
        "display" : "Proximal spinal muscular atrophy type 3"
      },
      {
        "code" : "83420",
        "display" : "Proximal spinal muscular atrophy type 4"
      },
      {
        "code" : "83450",
        "display" : "Regional odontodysplasia"
      },
      {
        "code" : "83451",
        "display" : "Florid cemento-osseous dysplasia"
      },
      {
        "code" : "83452",
        "display" : "Complex regional pain syndrome"
      },
      {
        "code" : "83453",
        "display" : "Vulvovaginal gingival syndrome"
      },
      {
        "code" : "83454",
        "display" : "Glomuvenous malformation"
      },
      {
        "code" : "83461",
        "display" : "Congenital primary aphakia"
      },
      {
        "code" : "83463",
        "display" : "Microtia"
      },
      {
        "code" : "83465",
        "display" : "Narcolepsy type 2"
      },
      {
        "code" : "83467",
        "display" : "Morvan syndrome"
      },
      {
        "code" : "83468",
        "display" : "Solitary bone cyst"
      },
      {
        "code" : "83469",
        "display" : "Desmoplastic small round cell tumor"
      },
      {
        "code" : "83471",
        "display" : "T-cell immunodeficiency with thymic aplasia"
      },
      {
        "code" : "83472",
        "display" : "CAMOS syndrome"
      },
      {
        "code" : "83473",
        "display" : "Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome"
      },
      {
        "code" : "83476",
        "display" : "West-Nile encephalitis"
      },
      {
        "code" : "83482",
        "display" : "Mycoplasma encephalitis"
      },
      {
        "code" : "83483",
        "display" : "La Crosse encephalitis"
      },
      {
        "code" : "83484",
        "display" : "St. Louis encephalitis"
      },
      {
        "code" : "83593",
        "display" : "Western equine encephalitis"
      },
      {
        "code" : "83594",
        "display" : "Eastern equine encephalitis"
      },
      {
        "code" : "83595",
        "display" : "Colorado tick fever"
      },
      {
        "code" : "83597",
        "display" : "Acute disseminated encephalomyelitis"
      },
      {
        "code" : "83600",
        "display" : "Encephalitis lethargica"
      },
      {
        "code" : "83601",
        "display" : "Steroid-responsive encephalopathy associated with autoimmune thyroiditis"
      },
      {
        "code" : "83616",
        "display" : "Rubella panencephalitis"
      },
      {
        "code" : "83617",
        "display" : "Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome"
      },
      {
        "code" : "83619",
        "display" : "Macrostomia-preauricular tags-external ophthalmoplegia syndrome"
      },
      {
        "code" : "83620",
        "display" : "Enteric anendocrinosis"
      },
      {
        "code" : "83628",
        "display" : "LUMBAR syndrome"
      },
      {
        "code" : "83629",
        "display" : "Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome"
      },
      {
        "code" : "83639",
        "display" : "Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency"
      },
      {
        "code" : "83642",
        "display" : "Microcytic anemia with liver iron overload"
      },
      {
        "code" : "838",
        "display" : "Susac syndrome"
      },
      {
        "code" : "839",
        "display" : "Congenital nephrotic syndrome, Finnish type"
      },
      {
        "code" : "84",
        "display" : "Fanconi anemia"
      },
      {
        "code" : "840",
        "display" : "Syringocystadenoma papilliferum"
      },
      {
        "code" : "84064",
        "display" : "Syndromic diarrhea"
      },
      {
        "code" : "84065",
        "display" : "Idiopathic malabsorption due to bile acid synthesis defects"
      },
      {
        "code" : "84081",
        "display" : "Senior-Boichis syndrome"
      },
      {
        "code" : "84085",
        "display" : "Hinman syndrome"
      },
      {
        "code" : "84087",
        "display" : "Collagen type III glomerulopathy"
      },
      {
        "code" : "84090",
        "display" : "Fibronectin glomerulopathy"
      },
      {
        "code" : "84093",
        "display" : "Hereditary thermosensitive neuropathy"
      },
      {
        "code" : "841",
        "display" : "Sebocystomatosis"
      },
      {
        "code" : "84132",
        "display" : "Desmin-related myopathy with Mallory body-like inclusions"
      },
      {
        "code" : "84142",
        "display" : "Isaacs syndrome"
      },
      {
        "code" : "842",
        "display" : "Testicular seminomatous germ cell tumor"
      },
      {
        "code" : "845",
        "display" : "Tay-Sachs disease"
      },
      {
        "code" : "846",
        "display" : "Alpha-thalassemia"
      },
      {
        "code" : "847",
        "display" : "X-linked alpha-thalassemia-intellectual disability syndrome"
      },
      {
        "code" : "848",
        "display" : "Beta-thalassemia"
      },
      {
        "code" : "849",
        "display" : "Glanzmann thrombasthenia"
      },
      {
        "code" : "851",
        "display" : "Paris-Trousseau thrombocytopenia"
      },
      {
        "code" : "85110",
        "display" : "Familial encephalopathy with neuroserpin inclusion bodies"
      },
      {
        "code" : "85112",
        "display" : "Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome"
      },
      {
        "code" : "85128",
        "display" : "Bothnia retinal dystrophy"
      },
      {
        "code" : "85136",
        "display" : "Cystic leukoencephalopathy without megalencephaly"
      },
      {
        "code" : "85138",
        "display" : "Addison disease"
      },
      {
        "code" : "85146",
        "display" : "Neurogenic scapuloperoneal syndrome, Kaeser type"
      },
      {
        "code" : "85162",
        "display" : "Facial onset sensory and motor neuronopathy"
      },
      {
        "code" : "85163",
        "display" : "Hypomyelination-congenital cataract syndrome"
      },
      {
        "code" : "85164",
        "display" : "Camptodactyly-tall stature-scoliosis-hearing loss syndrome"
      },
      {
        "code" : "85165",
        "display" : "Severe achondroplasia-developmental delay-acanthosis nigricans syndrome"
      },
      {
        "code" : "85166",
        "display" : "Platyspondylic dysplasia, Torrance type"
      },
      {
        "code" : "85167",
        "display" : "Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome"
      },
      {
        "code" : "85168",
        "display" : "Craniofacial conodysplasia"
      },
      {
        "code" : "85169",
        "display" : "Familial digital arthropathy-brachydactyly"
      },
      {
        "code" : "85170",
        "display" : "Mesomelic dysplasia, Savarirayan type"
      },
      {
        "code" : "85172",
        "display" : "Microcephalic osteodysplastic dysplasia, Saul-Wilson type"
      },
      {
        "code" : "85173",
        "display" : "IMAGe syndrome"
      },
      {
        "code" : "85174",
        "display" : "Pseudodiastrophic dysplasia"
      },
      {
        "code" : "85175",
        "display" : "Astley-Kendall dysplasia"
      },
      {
        "code" : "85179",
        "display" : "Infantile osteopetrosis with neuroaxonal dysplasia"
      },
      {
        "code" : "85182",
        "display" : "Diaphyseal medullary stenosis-bone malignancy syndrome"
      },
      {
        "code" : "85184",
        "display" : "Craniometadiaphyseal dysplasia, wormian bone type"
      },
      {
        "code" : "85186",
        "display" : "Endosteal sclerosis-cerebellar hypoplasia syndrome"
      },
      {
        "code" : "85188",
        "display" : "Metaphyseal dysplasia, Braun-Tinschert type"
      },
      {
        "code" : "85191",
        "display" : "Singleton-Merten dysplasia"
      },
      {
        "code" : "85192",
        "display" : "Calvarial doughnut lesions-bone fragility syndrome"
      },
      {
        "code" : "85193",
        "display" : "Idiopathic juvenile osteoporosis"
      },
      {
        "code" : "85194",
        "display" : "Spondylo-ocular syndrome"
      },
      {
        "code" : "85195",
        "display" : "Familial expansile osteolysis"
      },
      {
        "code" : "85197",
        "display" : "Genochondromatosis type 1"
      },
      {
        "code" : "85198",
        "display" : "Dysspondyloenchondromatosis"
      },
      {
        "code" : "85199",
        "display" : "Craniosynostosis-anal anomalies-porokeratosis syndrome"
      },
      {
        "code" : "852",
        "display" : "X-linked thrombocytopenia with normal platelets"
      },
      {
        "code" : "85201",
        "display" : "Genitopatellar syndrome"
      },
      {
        "code" : "85202",
        "display" : "Keutel syndrome"
      },
      {
        "code" : "85203",
        "display" : "Acropectoral syndrome"
      },
      {
        "code" : "85212",
        "display" : "Fetal Gaucher disease"
      },
      {
        "code" : "85273",
        "display" : "X-linked intellectual disability, Abidi type"
      },
      {
        "code" : "85274",
        "display" : "Syndromic X-linked intellectual disability 7"
      },
      {
        "code" : "85275",
        "display" : "Microphthalmia-ankyloblepharon-intellectual disability syndrome"
      },
      {
        "code" : "85276",
        "display" : "X-linked intellectual disability, Armfield type"
      },
      {
        "code" : "85277",
        "display" : "X-linked intellectual disability, Cantagrel type"
      },
      {
        "code" : "85278",
        "display" : "Christianson syndrome"
      },
      {
        "code" : "85279",
        "display" : "KDM5C-related syndromic X-linked intellectual disability"
      },
      {
        "code" : "85280",
        "display" : "X-linked intellectual disability-cubitus valgus-dysmorphism syndrome"
      },
      {
        "code" : "85282",
        "display" : "MEHMO syndrome"
      },
      {
        "code" : "85283",
        "display" : "X-linked intellectual disability, Miles-Carpenter type"
      },
      {
        "code" : "85284",
        "display" : "BRESEK syndrome"
      },
      {
        "code" : "85285",
        "display" : "X-linked intellectual disability, Schimke type"
      },
      {
        "code" : "85286",
        "display" : "X-linked intellectual disability, Shashi type"
      },
      {
        "code" : "85287",
        "display" : "X-linked intellectual disability, Siderius type"
      },
      {
        "code" : "85288",
        "display" : "X-linked intellectual disability, Stocco Dos Santos type"
      },
      {
        "code" : "85290",
        "display" : "X-linked intellectual disability, Wilson type"
      },
      {
        "code" : "85292",
        "display" : "X-linked spinocerebellar ataxia type 4"
      },
      {
        "code" : "85293",
        "display" : "X-linked intellectual disability, Cabezas type"
      },
      {
        "code" : "85294",
        "display" : "X-linked epilepsy-learning disabilities-behavior disorders syndrome"
      },
      {
        "code" : "85295",
        "display" : "HSD10 disease, atypical type"
      },
      {
        "code" : "85297",
        "display" : "X-linked spinocerebellar ataxia type 3"
      },
      {
        "code" : "853",
        "display" : "Fetal and neonatal alloimmune thrombocytopenia"
      },
      {
        "code" : "85317",
        "display" : "X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome"
      },
      {
        "code" : "85319",
        "display" : "X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome"
      },
      {
        "code" : "85320",
        "display" : "X-linked intellectual disability-macrocephaly-macroorchidism syndrome"
      },
      {
        "code" : "85321",
        "display" : "Deafness-intellectual disability syndrome, Martin-Probst type"
      },
      {
        "code" : "85322",
        "display" : "X-linked intellectual disability, Pai type"
      },
      {
        "code" : "85323",
        "display" : "X-linked intellectual disability, Seemanova type"
      },
      {
        "code" : "85324",
        "display" : "X-linked intellectual disability, Shrimpton type"
      },
      {
        "code" : "85325",
        "display" : "X-linked intellectual disability, Stevenson type"
      },
      {
        "code" : "85326",
        "display" : "X-linked intellectual disability, Stoll type"
      },
      {
        "code" : "85327",
        "display" : "X-linked intellectual disability-acromegaly-hyperactivity syndrome"
      },
      {
        "code" : "85329",
        "display" : "X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome"
      },
      {
        "code" : "85332",
        "display" : "X-linked intellectual disability-retinitis pigmentosa syndrome"
      },
      {
        "code" : "85334",
        "display" : "X-linked neurodegenerative syndrome, Bertini type"
      },
      {
        "code" : "85335",
        "display" : "Fried syndrome"
      },
      {
        "code" : "85336",
        "display" : "X-linked neurodegenerative syndrome, Hamel type"
      },
      {
        "code" : "85338",
        "display" : "X-linked intellectual disability-ataxia-apraxia syndrome"
      },
      {
        "code" : "854",
        "display" : "Non-malignant and non-cirrhotic portal vein thrombosis"
      },
      {
        "code" : "85408",
        "display" : "Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis"
      },
      {
        "code" : "85410",
        "display" : "Oligoarticular juvenile idiopathic arthritis"
      },
      {
        "code" : "85414",
        "display" : "Systemic-onset juvenile idiopathic arthritis"
      },
      {
        "code" : "85435",
        "display" : "Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis"
      },
      {
        "code" : "85436",
        "display" : "Psoriasis-related juvenile idiopathic arthritis"
      },
      {
        "code" : "85438",
        "display" : "Enthesitis-related juvenile idiopathic arthritis"
      },
      {
        "code" : "85442",
        "display" : "Short stature-pituitary and cerebellar defects-small sella turcica syndrome"
      },
      {
        "code" : "85443",
        "display" : "AL amyloidosis"
      },
      {
        "code" : "85445",
        "display" : "AA amyloidosis"
      },
      {
        "code" : "85446",
        "display" : "Wild type ABeta2M amyloidosis"
      },
      {
        "code" : "85447",
        "display" : "ATTRV30M amyloidosis"
      },
      {
        "code" : "85448",
        "display" : "AGel amyloidosis"
      },
      {
        "code" : "85450",
        "display" : "Hereditary amyloidosis with primary renal involvement"
      },
      {
        "code" : "85451",
        "display" : "ATTRV122I amyloidosis"
      },
      {
        "code" : "85453",
        "display" : "X-linked reticulate pigmentary disorder"
      },
      {
        "code" : "85458",
        "display" : "Cerebral Amyloid Angiopathy"
      },
      {
        "code" : "857",
        "display" : "Townes-Brocks syndrome"
      },
      {
        "code" : "858",
        "display" : "Congenital toxoplasmosis"
      },
      {
        "code" : "859",
        "display" : "Transcobalamin deficiency"
      },
      {
        "code" : "86",
        "display" : "Familial abdominal aortic aneurysm"
      },
      {
        "code" : "860",
        "display" : "Congenitally uncorrected transposition of the great arteries"
      },
      {
        "code" : "861",
        "display" : "Treacher-Collins syndrome"
      },
      {
        "code" : "863",
        "display" : "Trichinellosis"
      },
      {
        "code" : "86309",
        "display" : "DPAGT1-CDG"
      },
      {
        "code" : "864",
        "display" : "Trichofolliculoma"
      },
      {
        "code" : "867",
        "display" : "Familial multiple trichoepithelioma"
      },
      {
        "code" : "86788",
        "display" : "X-linked severe congenital neutropenia"
      },
      {
        "code" : "86789",
        "display" : "Isolated patella aplasia/hypoplasia"
      },
      {
        "code" : "86797",
        "display" : "Atypical lichen myxedematosus"
      },
      {
        "code" : "868",
        "display" : "Triose phosphate-isomerase deficiency"
      },
      {
        "code" : "86812",
        "display" : "POMT1-related limb-girdle muscular dystrophy R11"
      },
      {
        "code" : "86813",
        "display" : "Helicoid peripapillary chorioretinal degeneration"
      },
      {
        "code" : "86814",
        "display" : "Familial adult myoclonic epilepsy"
      },
      {
        "code" : "86815",
        "display" : "Aplasia of lacrimal and salivary glands"
      },
      {
        "code" : "86816",
        "display" : "Congenital analbuminemia"
      },
      {
        "code" : "86817",
        "display" : "Hemolytic anemia due to adenylate kinase deficiency"
      },
      {
        "code" : "86818",
        "display" : "Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome"
      },
      {
        "code" : "86819",
        "display" : "Atrichia with papular lesions"
      },
      {
        "code" : "86820",
        "display" : "Familial avascular necrosis of femoral head"
      },
      {
        "code" : "86821",
        "display" : "Lissencephaly type 3-familial fetal akinesia sequence syndrome"
      },
      {
        "code" : "86822",
        "display" : "Lissencephaly type 3-metacarpal bone dysplasia syndrome"
      },
      {
        "code" : "86829",
        "display" : "Chronic neutrophilic leukemia"
      },
      {
        "code" : "86830",
        "display" : "Chronic myeloproliferative disease, unclassifiable"
      },
      {
        "code" : "86834",
        "display" : "Juvenile myelomonocytic leukemia"
      },
      {
        "code" : "86839",
        "display" : "Myelodysplastic neoplasm with increased blasts"
      },
      {
        "code" : "86841",
        "display" : "Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality"
      },
      {
        "code" : "86843",
        "display" : "Acute panmyelosis with myelofibrosis"
      },
      {
        "code" : "86845",
        "display" : "Acute myeloid leukaemia with myelodysplasia-related features"
      },
      {
        "code" : "86849",
        "display" : "Acute basophilic leukemia"
      },
      {
        "code" : "86850",
        "display" : "Myeloid sarcoma"
      },
      {
        "code" : "86852",
        "display" : "B-cell prolymphocytic leukemia"
      },
      {
        "code" : "86854",
        "display" : "Splenic marginal zone lymphoma"
      },
      {
        "code" : "86855",
        "display" : "Plasmacytoma"
      },
      {
        "code" : "86861",
        "display" : "Non-amyloid monoclonal immunoglobulin deposition disease"
      },
      {
        "code" : "86864",
        "display" : "Heavy chain disease"
      },
      {
        "code" : "86867",
        "display" : "Nodal marginal zone B-cell lymphoma"
      },
      {
        "code" : "86869",
        "display" : "Lymphomatoid granulomatosis"
      },
      {
        "code" : "86870",
        "display" : "Blastic plasmacytoid dendritic cell neoplasm"
      },
      {
        "code" : "86871",
        "display" : "T-cell prolymphocytic leukemia"
      },
      {
        "code" : "86872",
        "display" : "T-cell large granular lymphocyte leukemia"
      },
      {
        "code" : "86873",
        "display" : "Aggressive NK-cell leukemia"
      },
      {
        "code" : "86875",
        "display" : "Adult T-cell leukemia/lymphoma"
      },
      {
        "code" : "86879",
        "display" : "Extranodal nasal NK/T cell lymphoma"
      },
      {
        "code" : "86880",
        "display" : "Enteropathy-associated T-cell lymphoma"
      },
      {
        "code" : "86882",
        "display" : "Hepatosplenic T-cell lymphoma"
      },
      {
        "code" : "86884",
        "display" : "Subcutaneous panniculitis-like T-cell lymphoma"
      },
      {
        "code" : "86885",
        "display" : "Primary cutaneous peripheral T-cell lymphoma not otherwise specified"
      },
      {
        "code" : "86886",
        "display" : "Angioimmunoblastic T-cell lymphoma"
      },
      {
        "code" : "86893",
        "display" : "Nodular lymphocyte predominant Hodgkin lymphoma"
      },
      {
        "code" : "86896",
        "display" : "Histiocytic sarcoma"
      },
      {
        "code" : "86897",
        "display" : "Langerhans cell sarcoma"
      },
      {
        "code" : "869",
        "display" : "Triple A syndrome"
      },
      {
        "code" : "86900",
        "display" : "Interdigitating dendritic cell sarcoma"
      },
      {
        "code" : "86902",
        "display" : "Follicular dendritic cell sarcoma"
      },
      {
        "code" : "86903",
        "display" : "Dendritic cell sarcoma not otherwise specified"
      },
      {
        "code" : "86904",
        "display" : "Methotrexate-associated lymphoproliferative disorders"
      },
      {
        "code" : "86906",
        "display" : "Gelastic seizures with hypothalamic hamartoma"
      },
      {
        "code" : "86908",
        "display" : "Hemiconvulsion-hemiplegia-epilepsy syndrome"
      },
      {
        "code" : "86909",
        "display" : "Myoclonic epilepsy of infancy"
      },
      {
        "code" : "86911",
        "display" : "Epilepsy with myoclonic absences"
      },
      {
        "code" : "86913",
        "display" : "Myoclonic epilepsy in non-progressive encephalopathies"
      },
      {
        "code" : "86914",
        "display" : "Lymphedema-cerebral arteriovenous anomaly-primary pulmonary hypertension syndrome"
      },
      {
        "code" : "86915",
        "display" : "Lymphedema-atrial septal defects-facial changes syndrome"
      },
      {
        "code" : "86918",
        "display" : "Diffuse palmoplantar keratoderma-acrocyanosis syndrome"
      },
      {
        "code" : "86919",
        "display" : "Keratosis palmaris et plantaris-clinodactyly syndrome"
      },
      {
        "code" : "86920",
        "display" : "Dermatopathia pigmentosa reticularis"
      },
      {
        "code" : "87",
        "display" : "Apert syndrome"
      },
      {
        "code" : "870",
        "display" : "Down syndrome"
      },
      {
        "code" : "871",
        "display" : "Hereditary progressive cardiac conduction defect"
      },
      {
        "code" : "873",
        "display" : "Desmoid tumor"
      },
      {
        "code" : "874",
        "display" : "Primary adult heart tumor"
      },
      {
        "code" : "875",
        "display" : "Primary pediatric heart tumor"
      },
      {
        "code" : "87503",
        "display" : "Mal de Meleda"
      },
      {
        "code" : "876",
        "display" : "Yolk sac tumor"
      },
      {
        "code" : "87876",
        "display" : "Sialidosis type 2"
      },
      {
        "code" : "87884",
        "display" : "Non-syndromic genetic deafness"
      },
      {
        "code" : "879",
        "display" : "Tungiasis"
      },
      {
        "code" : "88",
        "display" : "Idiopathic aplastic anemia"
      },
      {
        "code" : "881",
        "display" : "Turner syndrome"
      },
      {
        "code" : "882",
        "display" : "Tyrosinemia type 1"
      },
      {
        "code" : "883",
        "display" : "Extragonadal teratoma"
      },
      {
        "code" : "884",
        "display" : "Pallister-Killian syndrome"
      },
      {
        "code" : "886",
        "display" : "Usher syndrome"
      },
      {
        "code" : "88616",
        "display" : "Autosomal recessive non-syndromic intellectual disability"
      },
      {
        "code" : "88618",
        "display" : "S-adenosylhomocysteine hydrolase deficiency"
      },
      {
        "code" : "88619",
        "display" : "Familial acute necrotizing encephalopathy"
      },
      {
        "code" : "88620",
        "display" : "Isolated congenital anosmia"
      },
      {
        "code" : "88621",
        "display" : "Ichthyosis-prematurity syndrome"
      },
      {
        "code" : "88628",
        "display" : "Posterior column ataxia-retinitis pigmentosa syndrome"
      },
      {
        "code" : "88629",
        "display" : "Tritanopia"
      },
      {
        "code" : "88630",
        "display" : "Terminal osseous dysplasia-pigmentary defects syndrome"
      },
      {
        "code" : "88633",
        "display" : "Superior limbic keratoconjunctivitis"
      },
      {
        "code" : "88635",
        "display" : "Vacuolar myopathy with sarcoplasmic reticulum protein aggregates"
      },
      {
        "code" : "88637",
        "display" : "Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome"
      },
      {
        "code" : "88639",
        "display" : "Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency"
      },
      {
        "code" : "88642",
        "display" : "Congenital insensitivity to pain-anosmia-neuropathic arthropathy"
      },
      {
        "code" : "88643",
        "display" : "Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome"
      },
      {
        "code" : "88644",
        "display" : "Autosomal recessive ataxia, Beauce type"
      },
      {
        "code" : "88659",
        "display" : "Autosomal dominant progressive nephropathy with hypertension"
      },
      {
        "code" : "88660",
        "display" : "Hypertension due to gain-of-function mutations in the mineralocorticoid receptor"
      },
      {
        "code" : "88661",
        "display" : "Amelogenesis imperfecta"
      },
      {
        "code" : "887",
        "display" : "VACTERL/VATER association"
      },
      {
        "code" : "888",
        "display" : "Van der Woude syndrome"
      },
      {
        "code" : "889",
        "display" : "Cutaneous small vessel vasculitis"
      },
      {
        "code" : "88917",
        "display" : "X-linked Alport syndrome"
      },
      {
        "code" : "88918",
        "display" : "Autosomal dominant Alport syndrome"
      },
      {
        "code" : "88919",
        "display" : "Autosomal recessive Alport syndrome"
      },
      {
        "code" : "88924",
        "display" : "Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis"
      },
      {
        "code" : "88938",
        "display" : "Pseudohypoaldosteronism type 2A"
      },
      {
        "code" : "88939",
        "display" : "Pseudohypoaldosteronism type 2B"
      },
      {
        "code" : "88940",
        "display" : "Pseudohypoaldosteronism type 2C"
      },
      {
        "code" : "88949",
        "display" : "MUC1-related autosomal dominant tubulointerstitial kidney disease"
      },
      {
        "code" : "88950",
        "display" : "UMOD-related autosomal dominant tubulointerstitial kidney disease"
      },
      {
        "code" : "890",
        "display" : "Hepatic veno-occlusive disease"
      },
      {
        "code" : "891",
        "display" : "Familial exudative vitreoretinopathy"
      },
      {
        "code" : "892",
        "display" : "Von Hippel-Lindau disease"
      },
      {
        "code" : "893",
        "display" : "WAGR syndrome"
      },
      {
        "code" : "894",
        "display" : "Waardenburg syndrome type 1"
      },
      {
        "code" : "895",
        "display" : "Waardenburg syndrome type 2"
      },
      {
        "code" : "896",
        "display" : "Waardenburg syndrome type 3"
      },
      {
        "code" : "897",
        "display" : "Waardenburg-Shah syndrome"
      },
      {
        "code" : "898",
        "display" : "Wagner disease"
      },
      {
        "code" : "89838",
        "display" : "Autosomal recessive generalized epidermolysis bullosa simplex"
      },
      {
        "code" : "89842",
        "display" : "Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form"
      },
      {
        "code" : "89843",
        "display" : "Dystrophic epidermolysis bullosa pruriginosa"
      },
      {
        "code" : "89844",
        "display" : "Lissencephaly syndrome, Norman-Roberts type"
      },
      {
        "code" : "899",
        "display" : "Walker-Warburg syndrome"
      },
      {
        "code" : "89936",
        "display" : "X-linked hypophosphatemia"
      },
      {
        "code" : "89937",
        "display" : "Autosomal dominant hypophosphatemic rickets"
      },
      {
        "code" : "89938",
        "display" : "Bartter syndrome type 4"
      },
      {
        "code" : "9",
        "display" : "Tetrasomy X syndrome"
      },
      {
        "code" : "90",
        "display" : "Argininemia"
      },
      {
        "code" : "900",
        "display" : "Granulomatosis with polyangiitis"
      },
      {
        "code" : "90000",
        "display" : "Erythema elevatum diutinum"
      },
      {
        "code" : "90001",
        "display" : "X-linked cone dysfunction syndrome with myopia"
      },
      {
        "code" : "90002",
        "display" : "Undifferentiated connective tissue syndrome"
      },
      {
        "code" : "90003",
        "display" : "Inflammatory pseudotumor of the liver"
      },
      {
        "code" : "90020",
        "display" : "Parkinson-dementia complex of Guam"
      },
      {
        "code" : "90021",
        "display" : "Radiation myelitis"
      },
      {
        "code" : "90023",
        "display" : "Primary immunodeficiency syndrome due to P14/LAMTOR2 deficiency"
      },
      {
        "code" : "90024",
        "display" : "Deafness with labyrinthine aplasia, microtia, and microdontia"
      },
      {
        "code" : "90026",
        "display" : "Primary erythromelalgia"
      },
      {
        "code" : "90030",
        "display" : "Hemolytic anemia due to glutathione reductase deficiency"
      },
      {
        "code" : "90031",
        "display" : "Non-spherocytic hemolytic anemia due to hexokinase deficiency"
      },
      {
        "code" : "90033",
        "display" : "Autoimmune hemolytic anemia, warm type"
      },
      {
        "code" : "90035",
        "display" : "Paroxysmal cold hemoglobinuria"
      },
      {
        "code" : "90036",
        "display" : "Mixed-type autoimmune hemolytic anemia"
      },
      {
        "code" : "90037",
        "display" : "Drug-induced autoimmune hemolytic anemia"
      },
      {
        "code" : "90038",
        "display" : "Shiga toxin-associated hemolytic uremic syndrome"
      },
      {
        "code" : "90039",
        "display" : "Hemoglobin D disease"
      },
      {
        "code" : "90041",
        "display" : "Gaisböck syndrome"
      },
      {
        "code" : "90042",
        "display" : "Primary familial polycythemia"
      },
      {
        "code" : "90044",
        "display" : "Familial pseudohyperkalemia"
      },
      {
        "code" : "90045",
        "display" : "Hereditary folate malabsorption"
      },
      {
        "code" : "90050",
        "display" : "Retinopathy of prematurity"
      },
      {
        "code" : "90051",
        "display" : "Sepsis in premature infants"
      },
      {
        "code" : "90052",
        "display" : "Recurrent hepatitis C virus induced liver disease in liver transplant recipients"
      },
      {
        "code" : "90053",
        "display" : "Complications after hematopoietic stem cell transplantation"
      },
      {
        "code" : "90056",
        "display" : "Moderate and severe traumatic brain injury"
      },
      {
        "code" : "90058",
        "display" : "Spinal cord injury"
      },
      {
        "code" : "90059",
        "display" : "Sudden sensorineural hearing loss"
      },
      {
        "code" : "90060",
        "display" : "Diffuse alveolar hemorrhage"
      },
      {
        "code" : "90062",
        "display" : "Acute liver failure"
      },
      {
        "code" : "90064",
        "display" : "Acute peripheral arterial occlusion"
      },
      {
        "code" : "90065",
        "display" : "Acquired aneurysmal subarachnoid hemorrhage"
      },
      {
        "code" : "90066",
        "display" : "Pneumonia caused by Pseudomonas aeruginosa infection"
      },
      {
        "code" : "90068",
        "display" : "Cocaine intoxication"
      },
      {
        "code" : "90069",
        "display" : "Systemic monochloroacetate poisoning"
      },
      {
        "code" : "90073",
        "display" : "Hepatitis B reinfection following liver transplantation"
      },
      {
        "code" : "90076",
        "display" : "Partial deep dermal and full thickness burns"
      },
      {
        "code" : "90078",
        "display" : "Invasive infections due to vancomycin-resistant enterococci"
      },
      {
        "code" : "90080",
        "display" : "Scarring in glaucoma filtration surgical procedures"
      },
      {
        "code" : "90081",
        "display" : "AIDS wasting syndrome"
      },
      {
        "code" : "901",
        "display" : "Wells syndrome"
      },
      {
        "code" : "90103",
        "display" : "Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome"
      },
      {
        "code" : "90117",
        "display" : "Hereditary motor and sensory neuropathy, Okinawa type"
      },
      {
        "code" : "90118",
        "display" : "Severe early-onset axonal neuropathy due to MFN2 deficiency"
      },
      {
        "code" : "90119",
        "display" : "Hereditary motor and sensory neuropathy with acrodystrophy"
      },
      {
        "code" : "90120",
        "display" : "Hereditary motor and sensory neuropathy type 6"
      },
      {
        "code" : "90153",
        "display" : "Mandibuloacral dysplasia with type A lipodystrophy"
      },
      {
        "code" : "90154",
        "display" : "Mandibuloacral dysplasia with type B lipodystrophy"
      },
      {
        "code" : "90156",
        "display" : "Centrifugal lipodystrophy"
      },
      {
        "code" : "90157",
        "display" : "Drug-induced localized lipodystrophy"
      },
      {
        "code" : "90158",
        "display" : "Idiopathic localized lipodystrophy"
      },
      {
        "code" : "90159",
        "display" : "Panniculitis-induced localized lipodystrophy"
      },
      {
        "code" : "90160",
        "display" : "Pressure-induced localized lipoatrophy"
      },
      {
        "code" : "90186",
        "display" : "Meige disease"
      },
      {
        "code" : "902",
        "display" : "Werner syndrome"
      },
      {
        "code" : "90280",
        "display" : "Chilblain lupus"
      },
      {
        "code" : "90281",
        "display" : "Discoid lupus erythematosus"
      },
      {
        "code" : "90282",
        "display" : "Hypertrophic or verrucous lupus erythematosus"
      },
      {
        "code" : "90283",
        "display" : "Lupus erythematosus tumidus"
      },
      {
        "code" : "90285",
        "display" : "Lupus erythematosus panniculitis"
      },
      {
        "code" : "90289",
        "display" : "Localized scleroderma"
      },
      {
        "code" : "90291",
        "display" : "Systemic sclerosis"
      },
      {
        "code" : "903",
        "display" : "Von Willebrand disease"
      },
      {
        "code" : "90301",
        "display" : "Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome"
      },
      {
        "code" : "90307",
        "display" : "Parkes Weber syndrome"
      },
      {
        "code" : "90308",
        "display" : "Capillary-lymphatic-venous malformation with segmental distribution"
      },
      {
        "code" : "90321",
        "display" : "Cockayne syndrome type 1"
      },
      {
        "code" : "90322",
        "display" : "Cockayne syndrome type 2"
      },
      {
        "code" : "90324",
        "display" : "Cockayne syndrome type 3"
      },
      {
        "code" : "90340",
        "display" : "Blau syndrome"
      },
      {
        "code" : "90342",
        "display" : "Xeroderma pigmentosum variant"
      },
      {
        "code" : "90348",
        "display" : "Autosomal dominant cutis laxa"
      },
      {
        "code" : "90349",
        "display" : "Autosomal recessive cutis laxa type 1"
      },
      {
        "code" : "90354",
        "display" : "Brittle cornea syndrome"
      },
      {
        "code" : "90362",
        "display" : "Primary intestinal lymphangiectasia"
      },
      {
        "code" : "90363",
        "display" : "Secondary intestinal lymphangiectasia"
      },
      {
        "code" : "90368",
        "display" : "Hypotrichosis simplex of the scalp"
      },
      {
        "code" : "90389",
        "display" : "Telangiectasia macularis eruptiva perstans"
      },
      {
        "code" : "90390",
        "display" : "Anonychia-onychodystrophy syndrome"
      },
      {
        "code" : "90393",
        "display" : "Nodular lichen myxedematosus"
      },
      {
        "code" : "90394",
        "display" : "Discrete papular lichen myxedematosus"
      },
      {
        "code" : "90395",
        "display" : "Papular mucinosis of infancy"
      },
      {
        "code" : "90396",
        "display" : "Acral persistent papular mucinosis"
      },
      {
        "code" : "90397",
        "display" : "Self-healing papular mucinosis"
      },
      {
        "code" : "90398",
        "display" : "Localized lichen myxedematosus with mixed features of different subtypes"
      },
      {
        "code" : "90399",
        "display" : "Localized lichen myxedematosus with monoclonal gammopathy or systemic symptoms"
      },
      {
        "code" : "904",
        "display" : "Williams syndrome"
      },
      {
        "code" : "90400",
        "display" : "Scleromyxedema without monoclonal gammopathy"
      },
      {
        "code" : "905",
        "display" : "Wilson disease"
      },
      {
        "code" : "906",
        "display" : "Wiskott-Aldrich syndrome"
      },
      {
        "code" : "90625",
        "display" : "Rare X-linked non-syndromic sensorineural deafness type DFN"
      },
      {
        "code" : "90635",
        "display" : "Rare autosomal dominant non-syndromic sensorineural deafness type DFNA"
      },
      {
        "code" : "90636",
        "display" : "Rare autosomal recessive non-syndromic sensorineural deafness type DFNB"
      },
      {
        "code" : "90641",
        "display" : "Rare mitochondrial non-syndromic sensorineural deafness"
      },
      {
        "code" : "90646",
        "display" : "Deafness-hypogonadism syndrome"
      },
      {
        "code" : "90647",
        "display" : "Jervell and Lange-Nielsen syndrome"
      },
      {
        "code" : "90650",
        "display" : "Otopalatodigital syndrome type 1"
      },
      {
        "code" : "90652",
        "display" : "Otopalatodigital syndrome type 2"
      },
      {
        "code" : "90653",
        "display" : "Stickler syndrome type 1"
      },
      {
        "code" : "90654",
        "display" : "Stickler syndrome type 2"
      },
      {
        "code" : "90658",
        "display" : "Charcot-Marie-Tooth disease type 1E"
      },
      {
        "code" : "90673",
        "display" : "Hypothyroidism due to TSH receptor mutations"
      },
      {
        "code" : "90674",
        "display" : "Isolated thyroid-stimulating hormone deficiency"
      },
      {
        "code" : "90695",
        "display" : "Non-acquired panhypopituitarism"
      },
      {
        "code" : "90790",
        "display" : "Congenital lipoid adrenal hyperplasia due to STAR deficency"
      },
      {
        "code" : "90791",
        "display" : "Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency"
      },
      {
        "code" : "90793",
        "display" : "Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency"
      },
      {
        "code" : "90794",
        "display" : "Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency"
      },
      {
        "code" : "90795",
        "display" : "Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency"
      },
      {
        "code" : "90796",
        "display" : "46,XY difference of sex development due to isolated 17,20-lyase deficiency"
      },
      {
        "code" : "90797",
        "display" : "Partial androgen insensitivity syndrome"
      },
      {
        "code" : "908",
        "display" : "Fragile X syndrome"
      },
      {
        "code" : "909",
        "display" : "Cerebrotendinous xanthomatosis"
      },
      {
        "code" : "91",
        "display" : "Aromatase deficiency"
      },
      {
        "code" : "910",
        "display" : "Xeroderma pigmentosum"
      },
      {
        "code" : "911",
        "display" : "Combined immunodeficiency due to ZAP70 deficiency"
      },
      {
        "code" : "91127",
        "display" : "Adenovirus infection in immunocompromised patients"
      },
      {
        "code" : "91130",
        "display" : "Cardiomyopathy-hypotonia-lactic acidosis syndrome"
      },
      {
        "code" : "91131",
        "display" : "DK1-CDG"
      },
      {
        "code" : "91132",
        "display" : "Ichthyosis-hypotrichosis syndrome"
      },
      {
        "code" : "91135",
        "display" : "Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency"
      },
      {
        "code" : "91136",
        "display" : "Acquired monoclonal Ig light chain-associated Fanconi syndrome"
      },
      {
        "code" : "91138",
        "display" : "Cryoglobulinemic vasculitis"
      },
      {
        "code" : "91139",
        "display" : "Simple cryoglobulinemia"
      },
      {
        "code" : "91140",
        "display" : "Unspecified juvenile idiopathic arthritis"
      },
      {
        "code" : "912",
        "display" : "Zellweger syndrome"
      },
      {
        "code" : "913",
        "display" : "Zollinger-Ellison syndrome"
      },
      {
        "code" : "91347",
        "display" : "TSH-secreting pituitary adenoma"
      },
      {
        "code" : "91348",
        "display" : "Functioning gonadotropic adenoma"
      },
      {
        "code" : "91349",
        "display" : "Non-functioning pituitary adenoma"
      },
      {
        "code" : "91350",
        "display" : "Pituitary deficiency due to Rathke cleft cysts"
      },
      {
        "code" : "91351",
        "display" : "Pituitary dermoid and epidermoid cysts"
      },
      {
        "code" : "91352",
        "display" : "Germinoma of the central nervous system"
      },
      {
        "code" : "91354",
        "display" : "Pituitary deficiency due to empty sella turcica syndrome"
      },
      {
        "code" : "91355",
        "display" : "Sheehan syndrome"
      },
      {
        "code" : "91358",
        "display" : "Congenital esophageal diverticulum"
      },
      {
        "code" : "91359",
        "display" : "Chronic pneumonitis of infancy"
      },
      {
        "code" : "91364",
        "display" : "Non-specific interstitial pneumonia"
      },
      {
        "code" : "91387",
        "display" : "Familial thoracic aortic aneurysm and aortic dissection"
      },
      {
        "code" : "91396",
        "display" : "Isolated cryptophthalmia"
      },
      {
        "code" : "91397",
        "display" : "Isolated ankyloblepharon filiforme adnatum"
      },
      {
        "code" : "91411",
        "display" : "Congenital ptosis"
      },
      {
        "code" : "91412",
        "display" : "Marcus-Gunn syndrome"
      },
      {
        "code" : "91413",
        "display" : "Congenital Horner syndrome"
      },
      {
        "code" : "91414",
        "display" : "Pilomatrixoma"
      },
      {
        "code" : "91416",
        "display" : "Isolated congenital alacrima"
      },
      {
        "code" : "91481",
        "display" : "Ring dermoid of cornea"
      },
      {
        "code" : "91483",
        "display" : "Rieger anomaly"
      },
      {
        "code" : "91489",
        "display" : "Isolated congenital megalocornea"
      },
      {
        "code" : "91490",
        "display" : "Isolated congenital sclerocornea"
      },
      {
        "code" : "91491",
        "display" : "Congenital ectropion uveae"
      },
      {
        "code" : "91492",
        "display" : "Early onset non-syndromic cataract"
      },
      {
        "code" : "91494",
        "display" : "Macular coloboma-cleft palate-hallux valgus syndrome"
      },
      {
        "code" : "91495",
        "display" : "Persistent hyperplastic primary vitreous"
      },
      {
        "code" : "91496",
        "display" : "Snowflake vitreoretinal degeneration"
      },
      {
        "code" : "91498",
        "display" : "Familial congenital palsy of trochlear nerve"
      },
      {
        "code" : "915",
        "display" : "Aarskog-Scott syndrome"
      },
      {
        "code" : "91500",
        "display" : "Tubulointerstitial nephritis and uveitis syndrome"
      },
      {
        "code" : "91546",
        "display" : "Lyme disease"
      },
      {
        "code" : "91547",
        "display" : "Relapsing fever"
      },
      {
        "code" : "916",
        "display" : "Aase-Smith syndrome"
      },
      {
        "code" : "920",
        "display" : "Ablepharon macrostomia syndrome"
      },
      {
        "code" : "92050",
        "display" : "Congenital tufting enteropathy"
      },
      {
        "code" : "921",
        "display" : "Abruzzo-Erickson syndrome"
      },
      {
        "code" : "922",
        "display" : "Familial nasal acilia"
      },
      {
        "code" : "926",
        "display" : "Acatalasemia"
      },
      {
        "code" : "927",
        "display" : "Hyperammonemia due to N-acetylglutamate synthase deficiency"
      },
      {
        "code" : "929",
        "display" : "Achalasia-microcephaly syndrome"
      },
      {
        "code" : "93",
        "display" : "Aspartylglucosaminuria"
      },
      {
        "code" : "930",
        "display" : "Idiopathic achalasia"
      },
      {
        "code" : "931",
        "display" : "Isolated acheiropodia"
      },
      {
        "code" : "93100",
        "display" : "Renal agenesis, unilateral"
      },
      {
        "code" : "93101",
        "display" : "Renal hypoplasia"
      },
      {
        "code" : "93108",
        "display" : "Renal dysplasia"
      },
      {
        "code" : "93109",
        "display" : "Congenital megacalycosis"
      },
      {
        "code" : "93110",
        "display" : "Posterior urethral valve"
      },
      {
        "code" : "93111",
        "display" : "HNF1B-related autosomal dominant tubulointerstitial kidney disease"
      },
      {
        "code" : "93114",
        "display" : "Autosomal dominant intermediate Charcot-Marie-Tooth disease type E"
      },
      {
        "code" : "93126",
        "display" : "Pauci-immune glomerulonephritis"
      },
      {
        "code" : "93160",
        "display" : "Hypocalcemic vitamin D-resistant rickets"
      },
      {
        "code" : "93164",
        "display" : "Transient pseudohypoaldosteronism"
      },
      {
        "code" : "93172",
        "display" : "Renal dysplasia, unilateral"
      },
      {
        "code" : "93173",
        "display" : "Renal dysplasia, bilateral"
      },
      {
        "code" : "93176",
        "display" : "Unilateral congenital megacalycosis"
      },
      {
        "code" : "93177",
        "display" : "Congenital bilateral megacalycosis"
      },
      {
        "code" : "932",
        "display" : "Achondrogenesis"
      },
      {
        "code" : "93256",
        "display" : "Fragile X-associated tremor/ataxia syndrome"
      },
      {
        "code" : "93258",
        "display" : "Pfeiffer syndrome type 1"
      },
      {
        "code" : "93259",
        "display" : "Pfeiffer syndrome type 2"
      },
      {
        "code" : "93260",
        "display" : "Pfeiffer syndrome type 3"
      },
      {
        "code" : "93262",
        "display" : "Crouzon syndrome-acanthosis nigricans syndrome"
      },
      {
        "code" : "93267",
        "display" : "Cloverleaf skull-multiple congenital anomalies syndrome"
      },
      {
        "code" : "93268",
        "display" : "Short rib-polydactyly syndrome, Beemer-Langer type"
      },
      {
        "code" : "93269",
        "display" : "Short rib-polydactyly syndrome, Majewski type"
      },
      {
        "code" : "93270",
        "display" : "Short rib-polydactyly syndrome, Saldino-Noonan type"
      },
      {
        "code" : "93271",
        "display" : "Short rib-polydactyly syndrome, Verma-Naumoff type"
      },
      {
        "code" : "93274",
        "display" : "Thanatophoric dysplasia type 2"
      },
      {
        "code" : "93276",
        "display" : "Polyostotic fibrous dysplasia"
      },
      {
        "code" : "93277",
        "display" : "Monostotic fibrous dysplasia"
      },
      {
        "code" : "93279",
        "display" : "Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis"
      },
      {
        "code" : "93282",
        "display" : "Spondyloepimetaphyseal dysplasia, PAPSS2 type"
      },
      {
        "code" : "93283",
        "display" : "Spondyloepiphyseal dysplasia, Kimberley type"
      },
      {
        "code" : "93284",
        "display" : "Spondyloepiphyseal dysplasia tarda"
      },
      {
        "code" : "93292",
        "display" : "Adenoma of pancreas"
      },
      {
        "code" : "93293",
        "display" : "Okihiro syndrome"
      },
      {
        "code" : "93296",
        "display" : "Achondrogenesis type 2"
      },
      {
        "code" : "93297",
        "display" : "Hypochondrogenesis"
      },
      {
        "code" : "93298",
        "display" : "Achondrogenesis type 1B"
      },
      {
        "code" : "93299",
        "display" : "Achondrogenesis type 1A"
      },
      {
        "code" : "93302",
        "display" : "Brachyolmia, Maroteaux type"
      },
      {
        "code" : "93304",
        "display" : "Autosomal dominant brachyolmia"
      },
      {
        "code" : "93307",
        "display" : "Multiple epiphyseal dysplasia type 4"
      },
      {
        "code" : "93308",
        "display" : "Multiple epiphyseal dysplasia type 1"
      },
      {
        "code" : "93311",
        "display" : "Multiple epiphyseal dysplasia type 5"
      },
      {
        "code" : "93314",
        "display" : "Spondylometaphyseal dysplasia, Kozlowski type"
      },
      {
        "code" : "93315",
        "display" : "Spondylometaphyseal dysplasia, 'corner fracture' type"
      },
      {
        "code" : "93316",
        "display" : "Spondylometaphyseal dysplasia, Schmidt type"
      },
      {
        "code" : "93317",
        "display" : "Spondylometaphyseal dysplasia, Sedaghatian type"
      },
      {
        "code" : "93320",
        "display" : "Isolated ulnar hemimelia"
      },
      {
        "code" : "93321",
        "display" : "Isolated radial hemimelia"
      },
      {
        "code" : "93322",
        "display" : "Isolated tibial hemimelia"
      },
      {
        "code" : "93323",
        "display" : "Isolated fibular hemimelia"
      },
      {
        "code" : "93324",
        "display" : "Autosomal recessive Kenny-Caffey syndrome"
      },
      {
        "code" : "93325",
        "display" : "Autosomal dominant Kenny-Caffey syndrome"
      },
      {
        "code" : "93328",
        "display" : "Autosomal dominant omodysplasia"
      },
      {
        "code" : "93329",
        "display" : "Autosomal recessive omodysplasia"
      },
      {
        "code" : "93333",
        "display" : "Pelviscapular dysplasia"
      },
      {
        "code" : "93334",
        "display" : "Postaxial polydactyly type A"
      },
      {
        "code" : "93335",
        "display" : "Postaxial polydactyly type B"
      },
      {
        "code" : "93336",
        "display" : "Polydactyly of a triphalangeal thumb"
      },
      {
        "code" : "93337",
        "display" : "Polydactyly of an index finger"
      },
      {
        "code" : "93338",
        "display" : "Polysyndactyly"
      },
      {
        "code" : "93339",
        "display" : "Polydactyly of a biphalangeal thumb and/or hallux"
      },
      {
        "code" : "93346",
        "display" : "Spondyloepimetaphyseal dysplasia congenita, Strudwick type"
      },
      {
        "code" : "93347",
        "display" : "Anauxetic dysplasia"
      },
      {
        "code" : "93349",
        "display" : "X-linked spondyloepimetaphyseal dysplasia"
      },
      {
        "code" : "93351",
        "display" : "Spondyloepimetaphyseal dysplasia, Irapa type"
      },
      {
        "code" : "93352",
        "display" : "Spondyloepimetaphyseal dysplasia, Shohat type"
      },
      {
        "code" : "93356",
        "display" : "Spondyloepimetaphyseal dysplasia, Missouri type"
      },
      {
        "code" : "93357",
        "display" : "SPONASTRIME dysplasia"
      },
      {
        "code" : "93358",
        "display" : "Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome"
      },
      {
        "code" : "93360",
        "display" : "Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type"
      },
      {
        "code" : "93372",
        "display" : "Familial hypocalciuric hypercalcemia type 1"
      },
      {
        "code" : "93382",
        "display" : "Brachydactyly type A6"
      },
      {
        "code" : "93383",
        "display" : "Brachydactyly type B"
      },
      {
        "code" : "93384",
        "display" : "Brachydactyly type C"
      },
      {
        "code" : "93387",
        "display" : "Brachydactyly type E"
      },
      {
        "code" : "93388",
        "display" : "Brachydactyly type A1"
      },
      {
        "code" : "93394",
        "display" : "Brachydactyly type A4"
      },
      {
        "code" : "93396",
        "display" : "Brachydactyly type A2"
      },
      {
        "code" : "93397",
        "display" : "Brachydactyly type A7"
      },
      {
        "code" : "93398",
        "display" : "Genochondromatosis type 2"
      },
      {
        "code" : "93399",
        "display" : "Juvenile sialidosis type 2"
      },
      {
        "code" : "93400",
        "display" : "Congenital sialidosis type 2"
      },
      {
        "code" : "93402",
        "display" : "Syndactyly type 1"
      },
      {
        "code" : "93403",
        "display" : "Syndactyly type 2"
      },
      {
        "code" : "93404",
        "display" : "Syndactyly type 3"
      },
      {
        "code" : "93405",
        "display" : "Syndactyly type 4"
      },
      {
        "code" : "93406",
        "display" : "Syndactyly type 5"
      },
      {
        "code" : "93409",
        "display" : "Brachydactyly-syndactyly, Zhao type"
      },
      {
        "code" : "93473",
        "display" : "Hurler syndrome"
      },
      {
        "code" : "93474",
        "display" : "Scheie syndrome"
      },
      {
        "code" : "93476",
        "display" : "Hurler-Scheie syndrome"
      },
      {
        "code" : "935",
        "display" : "Short-limb skeletal dysplasia with severe combined immunodeficiency"
      },
      {
        "code" : "93552",
        "display" : "Pediatric systemic lupus erythematosus"
      },
      {
        "code" : "93554",
        "display" : "Mixed cryoglobulinemia type II"
      },
      {
        "code" : "93555",
        "display" : "Mixed cryoglobulinemia type III"
      },
      {
        "code" : "93556",
        "display" : "Heavy chain deposition disease"
      },
      {
        "code" : "93557",
        "display" : "Light and heavy chain deposition disease"
      },
      {
        "code" : "93558",
        "display" : "Light chain deposition disease"
      },
      {
        "code" : "93560",
        "display" : "AApoAI amyloidosis"
      },
      {
        "code" : "93561",
        "display" : "ALys amyloidosis"
      },
      {
        "code" : "93562",
        "display" : "AFib amyloidosis"
      },
      {
        "code" : "93568",
        "display" : "Juvenile polymyositis"
      },
      {
        "code" : "93571",
        "display" : "Dense deposit disease"
      },
      {
        "code" : "93581",
        "display" : "Atypical hemolytic uremic syndrome with anti-factor H antibodies"
      },
      {
        "code" : "93583",
        "display" : "Congenital thrombotic thrombocytopenic purpura"
      },
      {
        "code" : "93585",
        "display" : "Immune-mediated thrombotic thrombocytopenic purpura"
      },
      {
        "code" : "93589",
        "display" : "Late-onset nephronophthisis"
      },
      {
        "code" : "93591",
        "display" : "Infantile nephronophthisis"
      },
      {
        "code" : "93592",
        "display" : "Juvenile nephronophthisis"
      },
      {
        "code" : "93598",
        "display" : "Primary hyperoxaluria type 1"
      },
      {
        "code" : "93599",
        "display" : "Primary hyperoxaluria type 2"
      },
      {
        "code" : "93600",
        "display" : "Primary hyperoxaluria type 3"
      },
      {
        "code" : "93601",
        "display" : "Xanthinuria type I"
      },
      {
        "code" : "93602",
        "display" : "Xanthinuria type II"
      },
      {
        "code" : "93605",
        "display" : "Bartter syndrome type 3"
      },
      {
        "code" : "93606",
        "display" : "Nephrogenic syndrome of inappropriate antidiuresis"
      },
      {
        "code" : "93607",
        "display" : "Autosomal recessive proximal renal tubular acidosis"
      },
      {
        "code" : "93608",
        "display" : "Autosomal dominant distal renal tubular acidosis"
      },
      {
        "code" : "93610",
        "display" : "Distal renal tubular acidosis with anemia"
      },
      {
        "code" : "93612",
        "display" : "Cystinuria type A"
      },
      {
        "code" : "93613",
        "display" : "Cystinuria type B"
      },
      {
        "code" : "93616",
        "display" : "Hemoglobin H disease"
      },
      {
        "code" : "93622",
        "display" : "Dent disease type 1"
      },
      {
        "code" : "93623",
        "display" : "Dent disease type 2"
      },
      {
        "code" : "93672",
        "display" : "Juvenile dermatomyositis"
      },
      {
        "code" : "93685",
        "display" : "Unicentric Castleman disease"
      },
      {
        "code" : "939",
        "display" : "3-hydroxyisobutyric aciduria"
      },
      {
        "code" : "93921",
        "display" : "Full schwannomatosis"
      },
      {
        "code" : "93924",
        "display" : "Lobar holoprosencephaly"
      },
      {
        "code" : "93925",
        "display" : "Alobar holoprosencephaly"
      },
      {
        "code" : "93926",
        "display" : "Midline interhemispheric variant of holoprosencephaly"
      },
      {
        "code" : "93928",
        "display" : "Isolated epispadias"
      },
      {
        "code" : "93929",
        "display" : "Cloacal exstrophy"
      },
      {
        "code" : "93930",
        "display" : "Classic bladder exstrophy"
      },
      {
        "code" : "93932",
        "display" : "FG syndrome type 1"
      },
      {
        "code" : "93938",
        "display" : "Laryngotracheoesophageal cleft type 1"
      },
      {
        "code" : "93939",
        "display" : "Laryngotracheoesophageal cleft type 2"
      },
      {
        "code" : "93940",
        "display" : "Laryngotracheoesophageal cleft type 3"
      },
      {
        "code" : "93941",
        "display" : "Laryngotracheoesophageal cleft type 4"
      },
      {
        "code" : "93945",
        "display" : "X-linked intellectual disability, Porteous type"
      },
      {
        "code" : "93946",
        "display" : "Hamel cerebro-palato-cardiac syndrome"
      },
      {
        "code" : "93947",
        "display" : "X-linked intellectual disability, Golabi-Ito-Hall type"
      },
      {
        "code" : "93950",
        "display" : "X-linked intellectual disability, Sutherland-Haan type"
      },
      {
        "code" : "93952",
        "display" : "X-linked intellectual disability, Hedera type"
      },
      {
        "code" : "93953",
        "display" : "Familial thyroglossal duct cyst"
      },
      {
        "code" : "93958",
        "display" : "Oromandibular dystonia"
      },
      {
        "code" : "93964",
        "display" : "Blepharospasm-oromandibular dystonia syndrome"
      },
      {
        "code" : "93969",
        "display" : "Open spinal dysraphism with a myelomeningocele"
      },
      {
        "code" : "93976",
        "display" : "Anotia"
      },
      {
        "code" : "94056",
        "display" : "Isolated humero-ulnar synostosis"
      },
      {
        "code" : "94058",
        "display" : "Neovascular glaucoma"
      },
      {
        "code" : "94059",
        "display" : "Uremic pruritus"
      },
      {
        "code" : "94063",
        "display" : "12q14 microdeletion syndrome"
      },
      {
        "code" : "94064",
        "display" : "Deafness-infertility syndrome"
      },
      {
        "code" : "94065",
        "display" : "15q24 microdeletion syndrome"
      },
      {
        "code" : "94066",
        "display" : "Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia"
      },
      {
        "code" : "94068",
        "display" : "Spondyloepiphyseal dysplasia congenita"
      },
      {
        "code" : "94080",
        "display" : "Non-functioning paraganglioma"
      },
      {
        "code" : "94083",
        "display" : "Partington syndrome"
      },
      {
        "code" : "94086",
        "display" : "Blue diaper syndrome"
      },
      {
        "code" : "94087",
        "display" : "Cytophagic histiocytic panniculitis"
      },
      {
        "code" : "94088",
        "display" : "Hereditary renal hypouricemia"
      },
      {
        "code" : "94089",
        "display" : "Pseudohypoparathyroidism type 1B"
      },
      {
        "code" : "94090",
        "display" : "Pseudohypoparathyroidism type 2"
      },
      {
        "code" : "94091",
        "display" : "Mills syndrome"
      },
      {
        "code" : "94093",
        "display" : "Neuroleptic malignant syndrome"
      },
      {
        "code" : "941",
        "display" : "D-glyceric aciduria"
      },
      {
        "code" : "94122",
        "display" : "Cerebellar ataxia, Cayman type"
      },
      {
        "code" : "94124",
        "display" : "Spinocerebellar ataxia with axonal neuropathy type 1"
      },
      {
        "code" : "94125",
        "display" : "Recessive mitochondrial ataxia syndrome"
      },
      {
        "code" : "94147",
        "display" : "Spinocerebellar ataxia type 7"
      },
      {
        "code" : "94150",
        "display" : "Anonychia congenita totalis"
      },
      {
        "code" : "943",
        "display" : "Malonic aciduria"
      },
      {
        "code" : "945",
        "display" : "Acalvaria"
      },
      {
        "code" : "949",
        "display" : "Acrocraniofacial dysostosis"
      },
      {
        "code" : "95",
        "display" : "Friedreich ataxia"
      },
      {
        "code" : "950",
        "display" : "Acrodysostosis"
      },
      {
        "code" : "95159",
        "display" : "Hepatoerythropoietic porphyria"
      },
      {
        "code" : "952",
        "display" : "Acrofacial dysostosis, Weyers type"
      },
      {
        "code" : "95232",
        "display" : "Lissencephaly due to LIS1 mutation"
      },
      {
        "code" : "95409",
        "display" : "Acute adrenal insufficiency"
      },
      {
        "code" : "95427",
        "display" : "Secondary short bowel syndrome"
      },
      {
        "code" : "95428",
        "display" : "COG8-CDG"
      },
      {
        "code" : "95429",
        "display" : "Angioma serpiginosum"
      },
      {
        "code" : "95430",
        "display" : "Congenital tracheomalacia"
      },
      {
        "code" : "95431",
        "display" : "Twin to twin transfusion syndrome"
      },
      {
        "code" : "95433",
        "display" : "Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome"
      },
      {
        "code" : "95434",
        "display" : "Autosomal recessive cerebellar ataxia-movement disorder syndrome"
      },
      {
        "code" : "95443",
        "display" : "Mesocardia"
      },
      {
        "code" : "95448",
        "display" : "Congenital aortic valve atresia"
      },
      {
        "code" : "95455",
        "display" : "Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum"
      },
      {
        "code" : "95457",
        "display" : "Tricuspid valve agenesis"
      },
      {
        "code" : "95459",
        "display" : "Congenital tricuspid stenosis"
      },
      {
        "code" : "95461",
        "display" : "Straddling or overriding tricuspid valve"
      },
      {
        "code" : "95462",
        "display" : "Accessory tricuspid valve tissue"
      },
      {
        "code" : "95465",
        "display" : "Cleft mitral valve"
      },
      {
        "code" : "95474",
        "display" : "Double-orifice mitral valve"
      },
      {
        "code" : "95486",
        "display" : "Premature closure of the arterial duct"
      },
      {
        "code" : "95491",
        "display" : "Congenital coronary artery aneurysm"
      },
      {
        "code" : "95494",
        "display" : "Combined pituitary hormone deficiencies, genetic forms"
      },
      {
        "code" : "95496",
        "display" : "Pituitary stalk interruption syndrome"
      },
      {
        "code" : "955",
        "display" : "Hajdu-Cheney syndrome"
      },
      {
        "code" : "95507",
        "display" : "Congenital anomaly of hepatic vein"
      },
      {
        "code" : "95512",
        "display" : "Adenohypophysitis"
      },
      {
        "code" : "95513",
        "display" : "Panhypophysitis"
      },
      {
        "code" : "95613",
        "display" : "Pituitary apoplexy"
      },
      {
        "code" : "95619",
        "display" : "Post-traumatic pituitary deficiency"
      },
      {
        "code" : "95626",
        "display" : "Acquired arginine vasopressin deficiency"
      },
      {
        "code" : "95699",
        "display" : "Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency"
      },
      {
        "code" : "957",
        "display" : "Acropectorovertebral dysplasia"
      },
      {
        "code" : "95700",
        "display" : "Familial adrenal hypoplasia with absent pituitary luteinizing hormone"
      },
      {
        "code" : "95702",
        "display" : "X-linked adrenal hypoplasia congenita"
      },
      {
        "code" : "95706",
        "display" : "Non-syndromic posterior hypospadias"
      },
      {
        "code" : "95707",
        "display" : "Idiopathic isolated micropenis"
      },
      {
        "code" : "95712",
        "display" : "Thyroid ectopia"
      },
      {
        "code" : "95713",
        "display" : "Athyreosis"
      },
      {
        "code" : "95715",
        "display" : "Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies"
      },
      {
        "code" : "95716",
        "display" : "Familial thyroid dyshormonogenesis"
      },
      {
        "code" : "95717",
        "display" : "Idiopathic congenital hypothyroidism"
      },
      {
        "code" : "95719",
        "display" : "Thyroid hemiagenesis"
      },
      {
        "code" : "95720",
        "display" : "Thyroid hypoplasia"
      },
      {
        "code" : "958",
        "display" : "Acro-renal-mandibular syndrome"
      },
      {
        "code" : "95854",
        "display" : "Levocardia"
      },
      {
        "code" : "959",
        "display" : "Acro-renal-ocular syndrome"
      },
      {
        "code" : "96",
        "display" : "Ataxia with vitamin E deficiency"
      },
      {
        "code" : "96055",
        "display" : "Tetrasomy 21 syndrome"
      },
      {
        "code" : "96059",
        "display" : "Mosaic trisomy 4 syndrome"
      },
      {
        "code" : "96060",
        "display" : "Mosaic trisomy 5 syndrome"
      },
      {
        "code" : "96061",
        "display" : "Mosaic trisomy 8 syndrome"
      },
      {
        "code" : "96063",
        "display" : "Mosaic trisomy 10 syndrome"
      },
      {
        "code" : "96068",
        "display" : "Mosaic trisomy 22 syndrome"
      },
      {
        "code" : "96069",
        "display" : "Distal duplication 1p36 syndrome"
      },
      {
        "code" : "96070",
        "display" : "Distal duplication 2p syndrome"
      },
      {
        "code" : "96071",
        "display" : "Distal duplication 3p syndrome"
      },
      {
        "code" : "96072",
        "display" : "4p16.3 microduplication syndrome"
      },
      {
        "code" : "96074",
        "display" : "Distal duplication 7p syndrome"
      },
      {
        "code" : "96076",
        "display" : "Beckwith-Wiedemann syndrome due to 11p15 microduplication"
      },
      {
        "code" : "96078",
        "display" : "16p13.3 microduplication syndrome"
      },
      {
        "code" : "96092",
        "display" : "8p inverted duplication/deletion syndrome"
      },
      {
        "code" : "96094",
        "display" : "Distal duplication 2q syndrome"
      },
      {
        "code" : "96095",
        "display" : "3q26 microduplication syndrome"
      },
      {
        "code" : "96096",
        "display" : "Distal duplication 4q syndrome"
      },
      {
        "code" : "96097",
        "display" : "Distal duplication 5q syndrome"
      },
      {
        "code" : "96098",
        "display" : "Distal duplication 6q syndrome"
      },
      {
        "code" : "96100",
        "display" : "Distal duplication 8q syndrome"
      },
      {
        "code" : "96101",
        "display" : "Distal duplication 9q syndrome"
      },
      {
        "code" : "96102",
        "display" : "Distal duplication 10q syndrome"
      },
      {
        "code" : "96103",
        "display" : "Distal duplication 11q syndrome"
      },
      {
        "code" : "96105",
        "display" : "Distal duplication 13q syndrome"
      },
      {
        "code" : "96106",
        "display" : "Distal duplication 16q syndrome"
      },
      {
        "code" : "96107",
        "display" : "Distal duplication 20q syndrome"
      },
      {
        "code" : "96109",
        "display" : "Distal duplication 22q syndrome"
      },
      {
        "code" : "96112",
        "display" : "Non-distal duplication 9q syndrome"
      },
      {
        "code" : "96121",
        "display" : "7q11.23 microduplication syndrome"
      },
      {
        "code" : "96123",
        "display" : "Monosomy 22 syndrome"
      },
      {
        "code" : "96125",
        "display" : "Distal deletion 6p syndrome"
      },
      {
        "code" : "96126",
        "display" : "Distal deletion 7p syndrome"
      },
      {
        "code" : "96129",
        "display" : "Distal deletion 19p syndrome"
      },
      {
        "code" : "96145",
        "display" : "Distal deletion 4q syndrome"
      },
      {
        "code" : "96147",
        "display" : "Kleefstra syndrome due to 9q34 microdeletion"
      },
      {
        "code" : "96148",
        "display" : "Distal deletion 10q syndrome"
      },
      {
        "code" : "96149",
        "display" : "Distal deletion 12q syndrome"
      },
      {
        "code" : "96150",
        "display" : "Distal deletion 14q syndrome"
      },
      {
        "code" : "96160",
        "display" : "Non-distal deletion 12q syndrome"
      },
      {
        "code" : "96167",
        "display" : "Recombinant 8 syndrome"
      },
      {
        "code" : "96168",
        "display" : "Monosomy 13q34 syndrome"
      },
      {
        "code" : "96169",
        "display" : "Koolen-De Vries syndrome"
      },
      {
        "code" : "96170",
        "display" : "Emanuel syndrome"
      },
      {
        "code" : "96171",
        "display" : "Ring chromosome 2 syndrome"
      },
      {
        "code" : "96172",
        "display" : "Ring chromosome 3 syndrome"
      },
      {
        "code" : "96173",
        "display" : "Ring chromosome 9 syndrome"
      },
      {
        "code" : "96175",
        "display" : "Ring chromosome 11 syndrome"
      },
      {
        "code" : "96176",
        "display" : "Ring chromosome 13 syndrome"
      },
      {
        "code" : "96177",
        "display" : "Ring chromosome 15 syndrome"
      },
      {
        "code" : "96178",
        "display" : "Ring chromosome 16 syndrome"
      },
      {
        "code" : "96179",
        "display" : "Maternal uniparental disomy of chromosome 2 syndrome"
      },
      {
        "code" : "96180",
        "display" : "Maternal uniparental disomy of chromosome 4 syndrome"
      },
      {
        "code" : "96181",
        "display" : "Maternal uniparental disomy of chromosome 6 syndrome"
      },
      {
        "code" : "96182",
        "display" : "Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7"
      },
      {
        "code" : "96183",
        "display" : "Maternal uniparental disomy of chromosome 9 syndrome"
      },
      {
        "code" : "96184",
        "display" : "Temple syndrome due to maternal uniparental disomy of chromosome 14"
      },
      {
        "code" : "96185",
        "display" : "Maternal uniparental disomy of chromosome 16 syndrome"
      },
      {
        "code" : "96186",
        "display" : "Maternal uniparental disomy of chromosome 20 syndrome"
      },
      {
        "code" : "96187",
        "display" : "Maternal uniparental disomy of chromosome 21 syndrome"
      },
      {
        "code" : "96188",
        "display" : "Maternal uniparental disomy of chromosome 22 syndrome"
      },
      {
        "code" : "96190",
        "display" : "Paternal uniparental disomy of chromosome 5 syndrome"
      },
      {
        "code" : "96191",
        "display" : "Paternal uniparental disomy of chromosome 6 syndrome"
      },
      {
        "code" : "96192",
        "display" : "Paternal uniparental disomy of chromosome 7 syndrome"
      },
      {
        "code" : "96193",
        "display" : "Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11"
      },
      {
        "code" : "96194",
        "display" : "Paternal uniparental disomy of chromosome 20 syndrome"
      },
      {
        "code" : "96195",
        "display" : "Paternal uniparental disomy of chromosome 21 syndrome"
      },
      {
        "code" : "96201",
        "display" : "X small rings syndrome"
      },
      {
        "code" : "96253",
        "display" : "Cushing disease"
      },
      {
        "code" : "96263",
        "display" : "48,XXXY syndrome"
      },
      {
        "code" : "96264",
        "display" : "49,XXXXY syndrome"
      },
      {
        "code" : "96265",
        "display" : "Leydig cell hypoplasia due to complete LH resistance"
      },
      {
        "code" : "96266",
        "display" : "Leydig cell hypoplasia due to partial LH resistance"
      },
      {
        "code" : "96269",
        "display" : "Isolated partial vaginal agenesis"
      },
      {
        "code" : "963",
        "display" : "Acromegaly"
      },
      {
        "code" : "96334",
        "display" : "Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14"
      },
      {
        "code" : "968",
        "display" : "Acromesomelic dysplasia, Hunter-Thompson type"
      },
      {
        "code" : "969",
        "display" : "Acromicric dysplasia"
      },
      {
        "code" : "97",
        "display" : "Familial paroxysmal ataxia"
      },
      {
        "code" : "970",
        "display" : "Hereditary sensory and autonomic neuropathy type 2"
      },
      {
        "code" : "971",
        "display" : "Acrorenal syndrome"
      },
      {
        "code" : "972",
        "display" : "Hereditary continuous muscle fiber activity"
      },
      {
        "code" : "97214",
        "display" : "Eisenmenger syndrome"
      },
      {
        "code" : "97229",
        "display" : "Riboflavin transporter deficiency"
      },
      {
        "code" : "97230",
        "display" : "Solar urticaria"
      },
      {
        "code" : "97232",
        "display" : "Fingerprint body myopathy"
      },
      {
        "code" : "97234",
        "display" : "Glycogen storage disease due to phosphoglycerate mutase deficiency"
      },
      {
        "code" : "97238",
        "display" : "Rippling muscle disease"
      },
      {
        "code" : "97239",
        "display" : "Reducing body myopathy"
      },
      {
        "code" : "97240",
        "display" : "Zebra body myopathy"
      },
      {
        "code" : "97244",
        "display" : "Rigid spine syndrome"
      },
      {
        "code" : "97249",
        "display" : "Pontocerebellar hypoplasia type 3"
      },
      {
        "code" : "97252",
        "display" : "Mega-cisterna magna"
      },
      {
        "code" : "97261",
        "display" : "GRFoma"
      },
      {
        "code" : "97278",
        "display" : "PPoma"
      },
      {
        "code" : "97279",
        "display" : "Insulinoma"
      },
      {
        "code" : "97280",
        "display" : "Glucagonoma"
      },
      {
        "code" : "97282",
        "display" : "VIPoma"
      },
      {
        "code" : "97283",
        "display" : "Somatostatinoma"
      },
      {
        "code" : "97285",
        "display" : "Thyroid lymphoma"
      },
      {
        "code" : "97286",
        "display" : "Carney-Stratakis syndrome"
      },
      {
        "code" : "97287",
        "display" : "Bronchial neuroendocrine tumor"
      },
      {
        "code" : "97289",
        "display" : "Thymic neuroendocrine tumor"
      },
      {
        "code" : "97290",
        "display" : "Familial papillary thyroid carcinoma with renal papillary neoplasia"
      },
      {
        "code" : "97292",
        "display" : "Cardiogenic shock"
      },
      {
        "code" : "97297",
        "display" : "Bohring-Opitz syndrome"
      },
      {
        "code" : "973",
        "display" : "Isolated absence/hypoplasia of fingers excluding thumb, unilateral"
      },
      {
        "code" : "97330",
        "display" : "Thoracic outlet syndrome"
      },
      {
        "code" : "97332",
        "display" : "Kienbock disease"
      },
      {
        "code" : "97335",
        "display" : "Osgood-Schlatter disease"
      },
      {
        "code" : "97336",
        "display" : "Panner disease"
      },
      {
        "code" : "97337",
        "display" : "Sinding-Larsen-Johansson disease"
      },
      {
        "code" : "97338",
        "display" : "Melanoma of soft tissue"
      },
      {
        "code" : "97339",
        "display" : "Dural sinus malformation"
      },
      {
        "code" : "97340",
        "display" : "Hunter-McAlpine syndrome"
      },
      {
        "code" : "97341",
        "display" : "Persistent placoid maculopathy"
      },
      {
        "code" : "97345",
        "display" : "ABri amyloidosis"
      },
      {
        "code" : "97346",
        "display" : "ADan amyloidosis"
      },
      {
        "code" : "97349",
        "display" : "Postencephalitic parkinsonism"
      },
      {
        "code" : "97352",
        "display" : "Pellagra"
      },
      {
        "code" : "97353",
        "display" : "Dementia pugilistica"
      },
      {
        "code" : "97355",
        "display" : "Caribbean parkinsonism"
      },
      {
        "code" : "97360",
        "display" : "Robinow syndrome"
      },
      {
        "code" : "97361",
        "display" : "Renal hypoplasia, unilateral"
      },
      {
        "code" : "97362",
        "display" : "Renal hypoplasia, bilateral"
      },
      {
        "code" : "97363",
        "display" : "Unilateral multicystic dysplastic kidney"
      },
      {
        "code" : "97364",
        "display" : "Bilateral multicystic dysplastic kidney"
      },
      {
        "code" : "97366",
        "display" : "Multiloculated renal cyst"
      },
      {
        "code" : "97367",
        "display" : "Renal tubular dysgenesis due to twin-twin transfusion"
      },
      {
        "code" : "97368",
        "display" : "Drug-related renal tubular dysgenesis"
      },
      {
        "code" : "97369",
        "display" : "Renal tubular dysgenesis of genetic origin"
      },
      {
        "code" : "974",
        "display" : "Adams-Oliver syndrome"
      },
      {
        "code" : "97548",
        "display" : "Right sided atrial isomerism"
      },
      {
        "code" : "97560",
        "display" : "Primary membranous glomerulonephritis"
      },
      {
        "code" : "97563",
        "display" : "Pauci-immune glomerulonephritis with ANCA"
      },
      {
        "code" : "97564",
        "display" : "Pauci-immune glomerulonephritis without ANCA"
      },
      {
        "code" : "97566",
        "display" : "Non-amyloid fibrillary glomerulopathy"
      },
      {
        "code" : "97567",
        "display" : "Immunotactoid glomerulopathy"
      },
      {
        "code" : "97598",
        "display" : "Congenital renal artery stenosis"
      },
      {
        "code" : "976",
        "display" : "Adenine phosphoribosyltransferase deficiency"
      },
      {
        "code" : "97678",
        "display" : "Maternal uniparental disomy of chromosome 13 syndrome"
      },
      {
        "code" : "97685",
        "display" : "17q11 microdeletion syndrome"
      },
      {
        "code" : "977",
        "display" : "Adrenomyodystrophy"
      },
      {
        "code" : "978",
        "display" : "ADULT syndrome"
      },
      {
        "code" : "98",
        "display" : "Autosomal recessive spastic ataxia of Charlevoix-Saguenay"
      },
      {
        "code" : "980",
        "display" : "Absence of the pulmonary artery"
      },
      {
        "code" : "981",
        "display" : "Internal carotid absence"
      },
      {
        "code" : "98267",
        "display" : "Genetic non-syndromic obesity"
      },
      {
        "code" : "983",
        "display" : "Testicular regression syndrome"
      },
      {
        "code" : "984",
        "display" : "Pulmonary agenesis"
      },
      {
        "code" : "98434",
        "display" : "Hereditary combined deficiency of vitamin K-dependent clotting factors"
      },
      {
        "code" : "98606",
        "display" : "Syndromic orbital border hypoplasia"
      },
      {
        "code" : "98619",
        "display" : "Rare isolated myopia"
      },
      {
        "code" : "98673",
        "display" : "Autosomal dominant optic atrophy, classic form"
      },
      {
        "code" : "98676",
        "display" : "Autosomal recessive isolated optic atrophy"
      },
      {
        "code" : "98686",
        "display" : "Congenital trochlear nerve palsy"
      },
      {
        "code" : "98754",
        "display" : "Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15"
      },
      {
        "code" : "98755",
        "display" : "Spinocerebellar ataxia type 1"
      },
      {
        "code" : "98756",
        "display" : "Spinocerebellar ataxia type 2"
      },
      {
        "code" : "98757",
        "display" : "Spinocerebellar ataxia type 3"
      },
      {
        "code" : "98758",
        "display" : "Spinocerebellar ataxia type 6"
      },
      {
        "code" : "98759",
        "display" : "Spinocerebellar ataxia type 17"
      },
      {
        "code" : "98760",
        "display" : "Spinocerebellar ataxia type 8"
      },
      {
        "code" : "98761",
        "display" : "Spinocerebellar ataxia type 10"
      },
      {
        "code" : "98762",
        "display" : "Spinocerebellar ataxia type 12"
      },
      {
        "code" : "98763",
        "display" : "Spinocerebellar ataxia type 14"
      },
      {
        "code" : "98764",
        "display" : "Spinocerebellar ataxia type 27A"
      },
      {
        "code" : "98765",
        "display" : "Spinocerebellar ataxia type 4"
      },
      {
        "code" : "98766",
        "display" : "Spinocerebellar ataxia type 5"
      },
      {
        "code" : "98767",
        "display" : "Spinocerebellar ataxia type 11"
      },
      {
        "code" : "98768",
        "display" : "Spinocerebellar ataxia type 13"
      },
      {
        "code" : "98769",
        "display" : "Spinocerebellar ataxia type 15/16"
      },
      {
        "code" : "98771",
        "display" : "Spinocerebellar ataxia type 18"
      },
      {
        "code" : "98772",
        "display" : "Spinocerebellar ataxia type 19/22"
      },
      {
        "code" : "98773",
        "display" : "Spinocerebellar ataxia type 21"
      },
      {
        "code" : "98784",
        "display" : "Sleep-related hypermotor epilepsy"
      },
      {
        "code" : "98791",
        "display" : "Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16"
      },
      {
        "code" : "98793",
        "display" : "Prader-Willi syndrome due to paternal 15q11q13 deletion"
      },
      {
        "code" : "98794",
        "display" : "Angelman syndrome due to maternal 15q11q13 deletion"
      },
      {
        "code" : "98795",
        "display" : "Angelman syndrome due to paternal uniparental disomy of chromosome 15"
      },
      {
        "code" : "98797",
        "display" : "Isochromosomy Yp syndrome"
      },
      {
        "code" : "98798",
        "display" : "Isochromosomy Yq syndrome"
      },
      {
        "code" : "988",
        "display" : "Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome"
      },
      {
        "code" : "98805",
        "display" : "Primary dystonia, DYT4 type"
      },
      {
        "code" : "98806",
        "display" : "Primary dystonia, DYT6 type"
      },
      {
        "code" : "98807",
        "display" : "Primary dystonia, DYT13 type"
      },
      {
        "code" : "98808",
        "display" : "Autosomal dominant dopa-responsive dystonia"
      },
      {
        "code" : "98809",
        "display" : "Paroxysmal kinesigenic dyskinesia"
      },
      {
        "code" : "98810",
        "display" : "Paroxysmal non-kinesigenic dyskinesia"
      },
      {
        "code" : "98811",
        "display" : "Paroxysmal exertion-induced dyskinesia"
      },
      {
        "code" : "98813",
        "display" : "Hypohidrotic ectodermal dysplasia with immunodeficiency"
      },
      {
        "code" : "98815",
        "display" : "Self-limited epilepsy with autonomic seizures"
      },
      {
        "code" : "98816",
        "display" : "Childhood occipital visual epilepsy"
      },
      {
        "code" : "98818",
        "display" : "Landau-Kleffner syndrome"
      },
      {
        "code" : "98819",
        "display" : "Familial temporal lobe epilepsy"
      },
      {
        "code" : "98820",
        "display" : "Familial focal epilepsy with variable foci"
      },
      {
        "code" : "98823",
        "display" : "Chronic myelomonocytic leukemia"
      },
      {
        "code" : "98824",
        "display" : "Atypical chronic myeloid leukemia"
      },
      {
        "code" : "98825",
        "display" : "Unclassified myelodysplastic/myeloproliferative disease"
      },
      {
        "code" : "98826",
        "display" : "Myelodysplastic neoplasm with low blasts"
      },
      {
        "code" : "98827",
        "display" : "Unclassified myelodysplastic syndrome"
      },
      {
        "code" : "98829",
        "display" : "Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)"
      },
      {
        "code" : "98831",
        "display" : "Acute myeloid leukemia with 11q23 abnormalities"
      },
      {
        "code" : "98832",
        "display" : "Acute myeloid leukemia with minimal differentiation"
      },
      {
        "code" : "98833",
        "display" : "Acute myeloblastic leukemia without maturation"
      },
      {
        "code" : "98834",
        "display" : "Acute myeloblastic leukemia with maturation"
      },
      {
        "code" : "98835",
        "display" : "Acute undifferentiated leukemia"
      },
      {
        "code" : "98838",
        "display" : "Primary mediastinal large B-cell lymphoma"
      },
      {
        "code" : "98839",
        "display" : "Intravascular large B-cell lymphoma"
      },
      {
        "code" : "98841",
        "display" : "Anaplastic large cell lymphoma"
      },
      {
        "code" : "98842",
        "display" : "Lymphomatoid papulosis"
      },
      {
        "code" : "98843",
        "display" : "Classic Hodgkin lymphoma, nodular sclerosis type"
      },
      {
        "code" : "98844",
        "display" : "Classic Hodgkin lymphoma, mixed cellularity type"
      },
      {
        "code" : "98845",
        "display" : "Classic Hodgkin lymphoma, lymphocyte-rich type"
      },
      {
        "code" : "98846",
        "display" : "Classic Hodgkin lymphoma, lymphocyte-depleted type"
      },
      {
        "code" : "98848",
        "display" : "Indolent systemic mastocytosis"
      },
      {
        "code" : "98849",
        "display" : "Systemic mastocytosis with associated hematologic neoplasm"
      },
      {
        "code" : "98850",
        "display" : "Aggressive systemic mastocytosis"
      },
      {
        "code" : "98851",
        "display" : "Mast cell leukemia"
      },
      {
        "code" : "98852",
        "display" : "Desquamative interstitial pneumonia"
      },
      {
        "code" : "98853",
        "display" : "Autosomal dominant Emery-Dreifuss muscular dystrophy"
      },
      {
        "code" : "98855",
        "display" : "Autosomal recessive Emery-Dreifuss muscular dystrophy"
      },
      {
        "code" : "98856",
        "display" : "Charcot-Marie-Tooth disease type 2B1"
      },
      {
        "code" : "98863",
        "display" : "X-linked Emery-Dreifuss muscular dystrophy"
      },
      {
        "code" : "98868",
        "display" : "Southeast Asian ovalocytosis"
      },
      {
        "code" : "98869",
        "display" : "Congenital dyserythropoietic anemia type I"
      },
      {
        "code" : "98870",
        "display" : "Congenital dyserythropoietic anemia type III"
      },
      {
        "code" : "98871",
        "display" : "Transient erythroblastopenia of childhood"
      },
      {
        "code" : "98872",
        "display" : "Primary acquired pure red cell aplasia"
      },
      {
        "code" : "98873",
        "display" : "Congenital dyserythropoietic anemia type II"
      },
      {
        "code" : "98878",
        "display" : "Hemophilia A"
      },
      {
        "code" : "98879",
        "display" : "Hemophilia B"
      },
      {
        "code" : "98880",
        "display" : "Familial afibrinogenemia"
      },
      {
        "code" : "98881",
        "display" : "Familial dysfibrinogenemia"
      },
      {
        "code" : "98885",
        "display" : "Bleeding diathesis due to glycoprotein VI deficiency"
      },
      {
        "code" : "98886",
        "display" : "Bleeding diathesis due to integrin alpha2-beta1 deficiency"
      },
      {
        "code" : "98889",
        "display" : "Bilateral perisylvian polymicrogyria"
      },
      {
        "code" : "98890",
        "display" : "Early-onset X-linked optic atrophy"
      },
      {
        "code" : "98892",
        "display" : "Periventricular nodular heterotopia"
      },
      {
        "code" : "98893",
        "display" : "Congenital muscular dystrophy type 1B"
      },
      {
        "code" : "98895",
        "display" : "Becker muscular dystrophy"
      },
      {
        "code" : "98896",
        "display" : "Duchenne muscular dystrophy"
      },
      {
        "code" : "98897",
        "display" : "Oculopharyngodistal myopathy"
      },
      {
        "code" : "989",
        "display" : "Hypoglossia-hypodactyly syndrome"
      },
      {
        "code" : "98902",
        "display" : "Amish nemaline myopathy"
      },
      {
        "code" : "98904",
        "display" : "Congenital myopathy with excess of thin filaments"
      },
      {
        "code" : "98905",
        "display" : "Congenital multicore myopathy with external ophthalmoplegia"
      },
      {
        "code" : "98907",
        "display" : "Neutral lipid storage disease with ichthyosis"
      },
      {
        "code" : "98908",
        "display" : "Neutral lipid storage disease with myopathy"
      },
      {
        "code" : "98909",
        "display" : "Desminopathy"
      },
      {
        "code" : "98911",
        "display" : "Distal myotilinopathy"
      },
      {
        "code" : "98912",
        "display" : "Late-onset distal myopathy, Markesbery-Griggs type"
      },
      {
        "code" : "98913",
        "display" : "Postsynaptic congenital myasthenic syndromes"
      },
      {
        "code" : "98914",
        "display" : "Presynaptic congenital myasthenic syndromes"
      },
      {
        "code" : "98915",
        "display" : "Synaptic congenital myasthenic syndromes"
      },
      {
        "code" : "98916",
        "display" : "Acute inflammatory demyelinating polyradiculoneuropathy"
      },
      {
        "code" : "98917",
        "display" : "Acute motor and sensory axonal neuropathy"
      },
      {
        "code" : "98918",
        "display" : "Acute motor axonal neuropathy"
      },
      {
        "code" : "98919",
        "display" : "Miller Fisher syndrome"
      },
      {
        "code" : "98920",
        "display" : "Spinal muscular atrophy with respiratory distress type 1"
      },
      {
        "code" : "98922",
        "display" : "Blake pouch cyst"
      },
      {
        "code" : "98933",
        "display" : "Multiple system atrophy, parkinsonian type"
      },
      {
        "code" : "98934",
        "display" : "Huntington disease-like 2"
      },
      {
        "code" : "98938",
        "display" : "Colobomatous microphthalmia"
      },
      {
        "code" : "98942",
        "display" : "Coloboma of choroid and retina"
      },
      {
        "code" : "98943",
        "display" : "Coloboma of eye lens"
      },
      {
        "code" : "98944",
        "display" : "Coloboma of iris"
      },
      {
        "code" : "98945",
        "display" : "Coloboma of macula"
      },
      {
        "code" : "98946",
        "display" : "Coloboma of eyelid"
      },
      {
        "code" : "98947",
        "display" : "Coloboma of optic disc"
      },
      {
        "code" : "98948",
        "display" : "Congenital symblepharon"
      },
      {
        "code" : "98949",
        "display" : "Complete cryptophthalmia"
      },
      {
        "code" : "98950",
        "display" : "Partial cryptophthalmia"
      },
      {
        "code" : "98951",
        "display" : "Inverse Marcus-Gunn phenomenon"
      },
      {
        "code" : "98954",
        "display" : "Meesmann corneal dystrophy"
      },
      {
        "code" : "98955",
        "display" : "Lisch epithelial corneal dystrophy"
      },
      {
        "code" : "98956",
        "display" : "Epithelial basement membrane dystrophy"
      },
      {
        "code" : "98957",
        "display" : "Gelatinous drop-like corneal dystrophy"
      },
      {
        "code" : "98958",
        "display" : "Climatic droplet keratopathy"
      },
      {
        "code" : "98959",
        "display" : "Subepithelial mucinous corneal dystrophy"
      },
      {
        "code" : "98960",
        "display" : "Thiel-Behnke corneal dystrophy"
      },
      {
        "code" : "98961",
        "display" : "Reis-Bücklers corneal dystrophy"
      },
      {
        "code" : "98962",
        "display" : "Granular corneal dystrophy type I"
      },
      {
        "code" : "98963",
        "display" : "Granular corneal dystrophy type II"
      },
      {
        "code" : "98964",
        "display" : "Lattice corneal dystrophy type I"
      },
      {
        "code" : "98967",
        "display" : "Schnyder corneal dystrophy"
      },
      {
        "code" : "98969",
        "display" : "Macular corneal dystrophy"
      },
      {
        "code" : "98970",
        "display" : "Fleck corneal dystrophy"
      },
      {
        "code" : "98971",
        "display" : "Posterior amorphous corneal dystrophy"
      },
      {
        "code" : "98972",
        "display" : "Central cloudy dystrophy of François"
      },
      {
        "code" : "98973",
        "display" : "Posterior polymorphous corneal dystrophy"
      },
      {
        "code" : "98974",
        "display" : "Fuchs endothelial corneal dystrophy"
      },
      {
        "code" : "98976",
        "display" : "Congenital glaucoma"
      },
      {
        "code" : "98977",
        "display" : "Juvenile glaucoma"
      },
      {
        "code" : "98978",
        "display" : "Axenfeld anomaly"
      },
      {
        "code" : "98979",
        "display" : "Chandler syndrome"
      },
      {
        "code" : "98980",
        "display" : "Cogan-Reese syndrome"
      },
      {
        "code" : "98981",
        "display" : "Essential iris atrophy"
      },
      {
        "code" : "98984",
        "display" : "Pulverulent cataract"
      },
      {
        "code" : "98985",
        "display" : "Early-onset sutural cataract"
      },
      {
        "code" : "98988",
        "display" : "Early-onset anterior polar cataract"
      },
      {
        "code" : "98989",
        "display" : "Cerulean cataract"
      },
      {
        "code" : "98990",
        "display" : "Coralliform cataract"
      },
      {
        "code" : "98991",
        "display" : "Early-onset nuclear cataract"
      },
      {
        "code" : "98992",
        "display" : "Early-onset partial cataract"
      },
      {
        "code" : "98993",
        "display" : "Early-onset posterior polar cataract"
      },
      {
        "code" : "98994",
        "display" : "Total early-onset cataract"
      },
      {
        "code" : "98995",
        "display" : "Early-onset zonular cataract"
      },
      {
        "code" : "990",
        "display" : "Agnathia-holoprosencephaly-situs inversus syndrome"
      },
      {
        "code" : "99000",
        "display" : "Adult-onset foveomacular vitelliform dystrophy"
      },
      {
        "code" : "99001",
        "display" : "Butterfly-shaped pigment dystrophy"
      },
      {
        "code" : "99002",
        "display" : "Reticular dystrophy of the retinal pigment epithelium"
      },
      {
        "code" : "99003",
        "display" : "Multifocal pattern dystrophy simulating fundus flavimaculatus"
      },
      {
        "code" : "99004",
        "display" : "Fundus pulverulentus"
      },
      {
        "code" : "99013",
        "display" : "Spastic paraplegia type 7"
      },
      {
        "code" : "99014",
        "display" : "X-linked Charcot-Marie-Tooth disease type 5"
      },
      {
        "code" : "99015",
        "display" : "Spastic paraplegia type 2"
      },
      {
        "code" : "99027",
        "display" : "Adult-onset autosomal dominant leukodystrophy"
      },
      {
        "code" : "99042",
        "display" : "Congenitally uncorrected transposition of the great arteries with coarctation"
      },
      {
        "code" : "99043",
        "display" : "Double outlet right ventricle with subaortic or doubly committed ventricular septal defect with pulmonary stenosis"
      },
      {
        "code" : "99045",
        "display" : "Double outlet right ventricle with subpulmonary ventricular septal defect"
      },
      {
        "code" : "99046",
        "display" : "Double outlet right ventricle with non-committed subpulmonary ventricular septal defect"
      },
      {
        "code" : "99048",
        "display" : "Pulmonary valve agenesis-intact ventricular septum-persistent ductus arteriosus syndrome"
      },
      {
        "code" : "99049",
        "display" : "Pulmonary artery coming from patent ductus arteriosus"
      },
      {
        "code" : "99050",
        "display" : "Abnormal origin of right or left pulmonary artery from the aorta"
      },
      {
        "code" : "99051",
        "display" : "Discrete fixed membranous subaortic stenosis"
      },
      {
        "code" : "99052",
        "display" : "Discrete fibromuscular subaortic stenosis"
      },
      {
        "code" : "99053",
        "display" : "Tunnel subaortic stenosis"
      },
      {
        "code" : "99054",
        "display" : "Valvular pulmonary stenosis"
      },
      {
        "code" : "99055",
        "display" : "Congenital anomaly of the tricuspid valve chordae"
      },
      {
        "code" : "99056",
        "display" : "Parachute tricuspid valve"
      },
      {
        "code" : "99057",
        "display" : "Congenital mitral stenosis"
      },
      {
        "code" : "99058",
        "display" : "Hypoplasia of the mitral valve annulus"
      },
      {
        "code" : "99059",
        "display" : "Congenital supravalvular mitral ring"
      },
      {
        "code" : "99060",
        "display" : "Congenital unguarded mitral orifice"
      },
      {
        "code" : "99061",
        "display" : "Accessory mitral valve tissue"
      },
      {
        "code" : "99062",
        "display" : "Mitral valve agenesis"
      },
      {
        "code" : "99063",
        "display" : "Shone complex"
      },
      {
        "code" : "99064",
        "display" : "Straddling and/or overriding mitral valve"
      },
      {
        "code" : "99067",
        "display" : "Complete atrioventricular septal defect with ventricular hypoplasia"
      },
      {
        "code" : "99068",
        "display" : "Complete atrioventricular septal defect-tetralogy of Fallot"
      },
      {
        "code" : "99070",
        "display" : "Aorto-right ventricular tunnel"
      },
      {
        "code" : "99071",
        "display" : "Aorto-left ventricular tunnel"
      },
      {
        "code" : "99072",
        "display" : "Congenital patent ductus arteriosus aneurysm"
      },
      {
        "code" : "99075",
        "display" : "Encircling double aortic arch"
      },
      {
        "code" : "99076",
        "display" : "Persistent fifth aortic arch"
      },
      {
        "code" : "99077",
        "display" : "Kommerell diverticulum"
      },
      {
        "code" : "99078",
        "display" : "Neuhauser anomaly"
      },
      {
        "code" : "99079",
        "display" : "Cervical aortic arch"
      },
      {
        "code" : "99081",
        "display" : "Right aortic arch"
      },
      {
        "code" : "99082",
        "display" : "Dysphagia lusoria"
      },
      {
        "code" : "99083",
        "display" : "Pulmonary artery hypoplasia"
      },
      {
        "code" : "99084",
        "display" : "Peripheral pulmonary stenosis"
      },
      {
        "code" : "99087",
        "display" : "Coronary ostial stenosis or atresia"
      },
      {
        "code" : "99089",
        "display" : "Abnormal number of coronary ostia"
      },
      {
        "code" : "99090",
        "display" : "Malposition of a coronary ostium"
      },
      {
        "code" : "99092",
        "display" : "Interventricular septum aneurysm"
      },
      {
        "code" : "99094",
        "display" : "Laubry-Pezzi syndrome"
      },
      {
        "code" : "99095",
        "display" : "Congenital Gerbode defect"
      },
      {
        "code" : "99098",
        "display" : "Cor triatriatum dexter"
      },
      {
        "code" : "99099",
        "display" : "Cor triatriatum sinister"
      },
      {
        "code" : "991",
        "display" : "PAGOD syndrome"
      },
      {
        "code" : "99100",
        "display" : "Juxtaposition of the atrial appendages"
      },
      {
        "code" : "99101",
        "display" : "Ectasia of the right atrial appendage"
      },
      {
        "code" : "99102",
        "display" : "Ectasia of the left atrial appendage"
      },
      {
        "code" : "99103",
        "display" : "Atrial septal defect, ostium secundum type"
      },
      {
        "code" : "99104",
        "display" : "Atrial septal defect, coronary sinus type"
      },
      {
        "code" : "99105",
        "display" : "Atrial septal defect, sinus venosus type"
      },
      {
        "code" : "99106",
        "display" : "Atrial septal defect, ostium primum type"
      },
      {
        "code" : "99107",
        "display" : "Atrial septal aneurysm"
      },
      {
        "code" : "99109",
        "display" : "Persistent left superior vena cava connecting through coronary sinus to left-sided atrium"
      },
      {
        "code" : "99110",
        "display" : "Right superior vena cava connecting to left-sided atrium"
      },
      {
        "code" : "99111",
        "display" : "Persistent left superior vena cava connecting to the roof of left-sided atrium"
      },
      {
        "code" : "99112",
        "display" : "Absence of innominate vein"
      },
      {
        "code" : "99113",
        "display" : "Subaortic course of innominate vein"
      },
      {
        "code" : "99114",
        "display" : "Agenesis of the superior vena cava"
      },
      {
        "code" : "99117",
        "display" : "Coronary sinus stenosis"
      },
      {
        "code" : "99118",
        "display" : "Coronary sinus atresia"
      },
      {
        "code" : "99119",
        "display" : "Right inferior vena cava connecting to left-sided atrium"
      },
      {
        "code" : "99120",
        "display" : "Persistent eustachian valve"
      },
      {
        "code" : "99121",
        "display" : "Azygos continuation of the inferior vena cava"
      },
      {
        "code" : "99122",
        "display" : "Congenital stenosis of the inferior vena cava"
      },
      {
        "code" : "99123",
        "display" : "Inferior vena cava interruption without azygos continuation"
      },
      {
        "code" : "99124",
        "display" : "Congenital partial pulmonary venous return anomaly"
      },
      {
        "code" : "99125",
        "display" : "Congenital total pulmonary venous return anomaly"
      },
      {
        "code" : "99126",
        "display" : "Congenital pulmonary vein atresia"
      },
      {
        "code" : "99129",
        "display" : "Congenital complete agenesis of pericardium"
      },
      {
        "code" : "99130",
        "display" : "Congenital partial agenesis of pericardium"
      },
      {
        "code" : "99131",
        "display" : "Pleuro-pericardial cyst"
      },
      {
        "code" : "99135",
        "display" : "6-phosphogluconate dehydrogenase deficiency"
      },
      {
        "code" : "99138",
        "display" : "Hemolytic anemia due to erythrocyte adenosine deaminase overproduction"
      },
      {
        "code" : "99139",
        "display" : "Unstable hemoglobin disease"
      },
      {
        "code" : "99141",
        "display" : "Lymphedema-posterior choanal atresia syndrome"
      },
      {
        "code" : "99147",
        "display" : "Acquired von Willebrand syndrome"
      },
      {
        "code" : "99169",
        "display" : "Epiblepharon"
      },
      {
        "code" : "99170",
        "display" : "Tarsal kink syndrome"
      },
      {
        "code" : "99171",
        "display" : "Isolated congenital ectropion"
      },
      {
        "code" : "99172",
        "display" : "Euryblepharon"
      },
      {
        "code" : "99176",
        "display" : "Congenital eyelid retraction"
      },
      {
        "code" : "99177",
        "display" : "Isolated distichiasis"
      },
      {
        "code" : "99179",
        "display" : "Kandori fleck retina"
      },
      {
        "code" : "99226",
        "display" : "Monosomy X syndrome"
      },
      {
        "code" : "99228",
        "display" : "Mosaic monosomy X syndrome"
      },
      {
        "code" : "99324",
        "display" : "Paternal uniparental disomy of chromosome 13 syndrome"
      },
      {
        "code" : "99329",
        "display" : "48,XYYY syndrome"
      },
      {
        "code" : "99330",
        "display" : "49,XYYYY syndrome"
      },
      {
        "code" : "99361",
        "display" : "Isolated familial medullary thyroid carcinoma"
      },
      {
        "code" : "994",
        "display" : "Fetal akinesia deformation sequence"
      },
      {
        "code" : "99413",
        "display" : "Turner syndrome due to structural X chromosome anomalies"
      },
      {
        "code" : "99429",
        "display" : "Complete androgen insensitivity syndrome"
      },
      {
        "code" : "99642",
        "display" : "Spondyloepimetaphyseal dysplasia, Handigodu type"
      },
      {
        "code" : "99646",
        "display" : "Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria"
      },
      {
        "code" : "99657",
        "display" : "Primary dystonia, DYT2 type"
      },
      {
        "code" : "99672",
        "display" : "Fried's tooth and nail syndrome"
      },
      {
        "code" : "99688",
        "display" : "Dermotrichic syndrome"
      },
      {
        "code" : "99701",
        "display" : "Mesial temporal lobe epilepsy with hippocampal sclerosis"
      },
      {
        "code" : "99704",
        "display" : "Early-onset obesity-hyperphagia-severe developmental delay syndrome"
      },
      {
        "code" : "99710",
        "display" : "Punctate acrokeratoderma freckle-like pigmentation"
      },
      {
        "code" : "99718",
        "display" : "Leber plus disease"
      },
      {
        "code" : "99725",
        "display" : "Pituitary gigantism"
      },
      {
        "code" : "99731",
        "display" : "Isolated sulfite oxidase deficiency"
      },
      {
        "code" : "99732",
        "display" : "Sulfite oxidase deficiency due to molybdenum cofactor deficiency"
      },
      {
        "code" : "99734",
        "display" : "Myotonia fluctuans"
      },
      {
        "code" : "99735",
        "display" : "Myotonia permanens"
      },
      {
        "code" : "99736",
        "display" : "Acetazolamide-responsive myotonia"
      },
      {
        "code" : "99741",
        "display" : "King-Denborough syndrome"
      },
      {
        "code" : "99742",
        "display" : "Amish lethal microcephaly"
      },
      {
        "code" : "99745",
        "display" : "Typhoid"
      },
      {
        "code" : "99748",
        "display" : "Pontiac fever"
      },
      {
        "code" : "99749",
        "display" : "Kostmann syndrome"
      },
      {
        "code" : "99750",
        "display" : "Atypical progressive supranuclear palsy syndrome"
      },
      {
        "code" : "99756",
        "display" : "Alveolar rhabdomyosarcoma"
      },
      {
        "code" : "99757",
        "display" : "Embryonal rhabdomyosarcoma"
      },
      {
        "code" : "99771",
        "display" : "Bifid uvula"
      },
      {
        "code" : "99772",
        "display" : "Cleft velum"
      },
      {
        "code" : "99776",
        "display" : "Mosaic trisomy 9 syndrome"
      },
      {
        "code" : "99789",
        "display" : "Dentin dysplasia type I"
      },
      {
        "code" : "99791",
        "display" : "Dentin dysplasia type II"
      },
      {
        "code" : "99792",
        "display" : "Dentin dysplasia-sclerotic bones syndrome"
      },
      {
        "code" : "99796",
        "display" : "Subcortical band heterotopia"
      },
      {
        "code" : "99797",
        "display" : "Anodontia"
      },
      {
        "code" : "99798",
        "display" : "Oligodontia"
      },
      {
        "code" : "998",
        "display" : "Albinism-deafness syndrome"
      },
      {
        "code" : "99802",
        "display" : "Hemimegalencephaly"
      },
      {
        "code" : "99803",
        "display" : "Haddad syndrome"
      },
      {
        "code" : "99806",
        "display" : "Oculootodental syndrome"
      },
      {
        "code" : "99807",
        "display" : "PEHO-like syndrome"
      },
      {
        "code" : "99810",
        "display" : "Familial porencephaly"
      },
      {
        "code" : "99811",
        "display" : "Neuronal intestinal pseudoobstruction"
      },
      {
        "code" : "99812",
        "display" : "LIG4 syndrome"
      },
      {
        "code" : "99819",
        "display" : "Familial gestational hyperthyroidism"
      },
      {
        "code" : "99824",
        "display" : "Lassa fever"
      },
      {
        "code" : "99825",
        "display" : "Nipah virus disease"
      },
      {
        "code" : "99826",
        "display" : "Marburg hemorrhagic fever"
      },
      {
        "code" : "99827",
        "display" : "Crimean-Congo hemorrhagic fever"
      },
      {
        "code" : "99828",
        "display" : "Dengue fever"
      },
      {
        "code" : "99829",
        "display" : "Yellow fever"
      },
      {
        "code" : "99832",
        "display" : "Resistance to thyrotropin-releasing hormone syndrome"
      },
      {
        "code" : "99842",
        "display" : "Leukocyte adhesion deficiency type I"
      },
      {
        "code" : "99843",
        "display" : "Leukocyte adhesion deficiency type II"
      },
      {
        "code" : "99844",
        "display" : "Leukocyte adhesion deficiency type III"
      },
      {
        "code" : "99845",
        "display" : "Genetic recurrent myoglobinuria"
      },
      {
        "code" : "99846",
        "display" : "Autosomal dominant myoglobinuria"
      },
      {
        "code" : "99849",
        "display" : "Glycogen storage disease due to muscle beta-enolase deficiency"
      },
      {
        "code" : "99852",
        "display" : "Ravine syndrome"
      },
      {
        "code" : "99853",
        "display" : "Ovarioleukodystrophy"
      },
      {
        "code" : "99854",
        "display" : "Cree leukoencephalopathy"
      },
      {
        "code" : "99856",
        "display" : "Primary syringomyelia"
      },
      {
        "code" : "99857",
        "display" : "Secondary syringomyelia"
      },
      {
        "code" : "99858",
        "display" : "Idiopathic syringomyelia"
      },
      {
        "code" : "99860",
        "display" : "Precursor B-cell acute lymphoblastic leukemia"
      },
      {
        "code" : "99861",
        "display" : "Precursor T-cell acute lymphoblastic leukemia"
      },
      {
        "code" : "99865",
        "display" : "Spermatocytic seminoma"
      },
      {
        "code" : "99867",
        "display" : "Thymoma"
      },
      {
        "code" : "99868",
        "display" : "Thymic carcinoma"
      },
      {
        "code" : "99869",
        "display" : "Thymic neuroendocrine carcinoma"
      },
      {
        "code" : "99879",
        "display" : "Familial isolated hyperparathyroidism"
      },
      {
        "code" : "99880",
        "display" : "Hyperparathyroidism-jaw tumor syndrome"
      },
      {
        "code" : "99885",
        "display" : "Isolated permanent neonatal diabetes mellitus"
      },
      {
        "code" : "99886",
        "display" : "Transient neonatal diabetes mellitus"
      },
      {
        "code" : "99887",
        "display" : "Acute megakaryoblastic leukemia in children with Down syndrome"
      },
      {
        "code" : "99889",
        "display" : "Cushing syndrome due to ectopic ACTH secretion"
      },
      {
        "code" : "99898",
        "display" : "Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency"
      },
      {
        "code" : "999",
        "display" : "Ermine phenotype"
      },
      {
        "code" : "99901",
        "display" : "Acyl-CoA dehydrogenase 9 deficiency"
      },
      {
        "code" : "99903",
        "display" : "Spirillary rat-bite fever"
      },
      {
        "code" : "99905",
        "display" : "Streptobacillary rat-bite fever"
      },
      {
        "code" : "99912",
        "display" : "Ovarian dysgerminoma"
      },
      {
        "code" : "99914",
        "display" : "Gynandroblastoma"
      },
      {
        "code" : "99915",
        "display" : "Malignant granulosa cell tumor of the ovary"
      },
      {
        "code" : "99916",
        "display" : "Malignant Sertoli-Leydig cell tumor of the ovary"
      },
      {
        "code" : "99917",
        "display" : "Theca steroid-producing cell malignant tumor of ovary, not further specified"
      },
      {
        "code" : "99918",
        "display" : "Streptococcal toxic-shock syndrome"
      },
      {
        "code" : "99919",
        "display" : "Staphylococcal toxic-shock syndrome"
      },
      {
        "code" : "99920",
        "display" : "Acute graft versus host disease"
      },
      {
        "code" : "99921",
        "display" : "Chronic graft versus host disease"
      },
      {
        "code" : "99922",
        "display" : "Ocular cicatricial pemphigoid"
      },
      {
        "code" : "99925",
        "display" : "Invasive mole"
      },
      {
        "code" : "99926",
        "display" : "Gestational choriocarcinoma"
      },
      {
        "code" : "99927",
        "display" : "Hydatidiform mole"
      },
      {
        "code" : "99928",
        "display" : "Placental site trophoblastic tumor"
      },
      {
        "code" : "99930",
        "display" : "Secondary pulmonary hemosiderosis"
      },
      {
        "code" : "99931",
        "display" : "Idiopathic pulmonary hemosiderosis"
      },
      {
        "code" : "99932",
        "display" : "Heiner syndrome"
      },
      {
        "code" : "99933",
        "display" : "Pleuropulmonary blastoma type 1"
      },
      {
        "code" : "99934",
        "display" : "Pleuropulmonary blastoma type 2"
      },
      {
        "code" : "99935",
        "display" : "Pleuropulmonary blastoma type 3"
      },
      {
        "code" : "99936",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2B"
      },
      {
        "code" : "99937",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2C"
      },
      {
        "code" : "99938",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2D"
      },
      {
        "code" : "99939",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2E"
      },
      {
        "code" : "99940",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2F"
      },
      {
        "code" : "99942",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2I"
      },
      {
        "code" : "99943",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2J"
      },
      {
        "code" : "99944",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2K"
      },
      {
        "code" : "99945",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2L"
      },
      {
        "code" : "99946",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2A1"
      },
      {
        "code" : "99947",
        "display" : "Autosomal dominant Charcot-Marie-Tooth disease type 2A2"
      },
      {
        "code" : "99948",
        "display" : "Charcot-Marie-Tooth disease type 4A"
      },
      {
        "code" : "99949",
        "display" : "Charcot-Marie-Tooth disease type 4C"
      },
      {
        "code" : "99950",
        "display" : "Charcot-Marie-Tooth disease type 4D"
      },
      {
        "code" : "99951",
        "display" : "Charcot-Marie-Tooth disease type 4E"
      },
      {
        "code" : "99952",
        "display" : "Charcot-Marie-Tooth disease type 4F"
      },
      {
        "code" : "99953",
        "display" : "Charcot-Marie-Tooth disease type 4G"
      },
      {
        "code" : "99954",
        "display" : "Charcot-Marie-Tooth disease type 4H"
      },
      {
        "code" : "99955",
        "display" : "Charcot-Marie-Tooth disease type 4B1"
      },
      {
        "code" : "99956",
        "display" : "Charcot-Marie-Tooth disease type 4B2"
      },
      {
        "code" : "99960",
        "display" : "Benign recurrent intrahepatic cholestasis type 1"
      },
      {
        "code" : "99961",
        "display" : "Benign recurrent intrahepatic cholestasis type 2"
      },
      {
        "code" : "99965",
        "display" : "O'Sullivan-McLeod syndrome"
      },
      {
        "code" : "99966",
        "display" : "Atypical teratoid rhabdoid tumor"
      },
      {
        "code" : "99967",
        "display" : "Myxoid/round cell liposarcoma"
      },
      {
        "code" : "99969",
        "display" : "Pleomorphic liposarcoma"
      },
      {
        "code" : "99970",
        "display" : "Dedifferentiated liposarcoma"
      },
      {
        "code" : "99971",
        "display" : "Well-differentiated liposarcoma"
      },
      {
        "code" : "99976",
        "display" : "Adenocarcinoma of the oesophagus and oesophagogastric junction"
      },
      {
        "code" : "99977",
        "display" : "Squamous cell carcinoma of the esophagus"
      },
      {
        "code" : "99978",
        "display" : "Perihilar cholangiocarcinoma"
      },
      {
        "code" : "99981",
        "display" : "Apnea of prematurity"
      },
      {
        "code" : "99989",
        "display" : "Intermediate DEND syndrome"
      },
      {
        "code" : "99990",
        "display" : "Brill-Zinsser disease"
      },
      {
        "code" : "99991",
        "display" : "Relapsing epidemic typhus"
      },
      {
        "code" : "99994",
        "display" : "Complex regional pain syndrome type 2"
      },
      {
        "code" : "99995",
        "display" : "Complex regional pain syndrome type 1"
      }]
    }]
  }
}

```
