# eHDSI Blood Group Laboratory - MyHealth@Eu MVC package v9.1.0

* [**Table of Contents**](toc.md)
* [**Artifacts Summary**](artifacts.md)
* **eHDSI Blood Group Laboratory**

## ValueSet: eHDSI Blood Group Laboratory 

| | |
| :--- | :--- |
| *Official URL*:http://terminology.ehdsi.eu/ValueSet/eHDSIBloodGroupLab | *Version*:9.1.0 |
| Active as of 2026-05-08 | *Computable Name*:EHDSIBloodGroupLab |
| *Other Identifiers:*OID:1.3.6.1.4.1.12559.11.10.1.3.1.42.105 | |
| **Copyright/Legal**: The Value Set incorporates SNOMED CT®, used by permission of the International Health Terminology Standards Development Organisation, trading as SNOMED International. SNOMED CT was originally created by the College of American Pathologists. SNOMED CT is a registered trademark of the International Health Terminology Standards Development Organisation, all rights reserved. For further information on the use of SNOMED CT, including translations, implementers of MyHealth@EU should review usage terms or directly contact SNOMED International: info@snomed.org. | |

 
The Value Set is used to code the value of patient’s blood group + Rh. 

 **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

-------

 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" : "eHDSIBloodGroupLab",
  "url" : "http://terminology.ehdsi.eu/ValueSet/eHDSIBloodGroupLab",
  "identifier" : [{
    "system" : "urn:ietf:rfc:3986",
    "value" : "urn:oid:1.3.6.1.4.1.12559.11.10.1.3.1.42.105"
  }],
  "version" : "9.1.0",
  "name" : "EHDSIBloodGroupLab",
  "title" : "eHDSI Blood Group Laboratory",
  "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 code the value of patient’s blood group + Rh.",
  "copyright" : "The Value Set incorporates SNOMED CT®, used by permission of the International Health Terminology Standards Development Organisation, trading as SNOMED International. SNOMED CT was originally created by the College of American Pathologists. SNOMED CT is a registered trademark of the International Health Terminology Standards Development Organisation, all rights reserved. For further information on the use of SNOMED CT, including translations, implementers of MyHealth@EU should review usage terms or directly contact SNOMED International: info@snomed.org.",
  "compose" : {
    "include" : [{
      "system" : "http://snomed.info/sct",
      "concept" : [{
        "code" : "103225004",
        "display" : "P>2< phenotype"
      },
      {
        "code" : "112143006",
        "display" : "ABO group phenotype"
      },
      {
        "code" : "112144000",
        "display" : "Blood group A"
      },
      {
        "code" : "112149005",
        "display" : "Blood group B"
      },
      {
        "code" : "115730009",
        "display" : "Hh blood group phenotype"
      },
      {
        "code" : "115731008",
        "display" : "Blood group O>h< Bombay"
      },
      {
        "code" : "115732001",
        "display" : "Blood group O>h< Bombay Indian type"
      },
      {
        "code" : "115734000",
        "display" : "Blood group O>h< Bombay Reunion type"
      },
      {
        "code" : "115735004",
        "display" : "Blood group Para-Bombay"
      },
      {
        "code" : "115736003",
        "display" : "Blood group A>h<"
      },
      {
        "code" : "115737007",
        "display" : "Blood group B>h<"
      },
      {
        "code" : "115748000",
        "display" : "Lewis blood group phenotype"
      },
      {
        "code" : "115749008",
        "display" : "Le(a-b-) phenotype"
      },
      {
        "code" : "115750008",
        "display" : "I blood group phenotype"
      },
      {
        "code" : "115751007",
        "display" : "i>cord< phenotype"
      },
      {
        "code" : "115752000",
        "display" : "i>adult< phenotype"
      },
      {
        "code" : "115753005",
        "display" : "i>1< phenotype"
      },
      {
        "code" : "115754004",
        "display" : "i>2< phenotype"
      },
      {
        "code" : "115755003",
        "display" : "I phenotype"
      },
      {
        "code" : "115756002",
        "display" : "I>int< phenotype"
      },
      {
        "code" : "115758001",
        "display" : "Rh (Rhesus) blood group phenotype"
      },
      {
        "code" : "115759009",
        "display" : "Rh>null< phenotype"
      },
      {
        "code" : "115760004",
        "display" : "X^o^rX^o^r blood group phenotype"
      },
      {
        "code" : "115761000",
        "display" : "Rr^-^ blood group phenotype"
      },
      {
        "code" : "115762007",
        "display" : "Rh>mod< blood group phenotype"
      },
      {
        "code" : "115763002",
        "display" : "Trans weak D phenotype"
      },
      {
        "code" : "115764008",
        "display" : "Inherited weak D phenotype"
      },
      {
        "code" : "115794002",
        "display" : "P blood group phenotype"
      },
      {
        "code" : "115795001",
        "display" : "P>1< phenotype"
      },
      {
        "code" : "115796000",
        "display" : "P>1<^k^ phenotype"
      },
      {
        "code" : "115797009",
        "display" : "P>2<^k^ phenotype"
      },
      {
        "code" : "115798004",
        "display" : "Landsteiner-Wiener phenotype"
      },
      {
        "code" : "115799007",
        "display" : "LW(a-b-) phenotype"
      },
      {
        "code" : "115800006",
        "display" : "MNS blood group phenotype"
      },
      {
        "code" : "115801005",
        "display" : "M^k^M^k^ phenotype"
      },
      {
        "code" : "115802003",
        "display" : "U- phenotype"
      },
      {
        "code" : "115803008",
        "display" : "En(a-) phenotype"
      },
      {
        "code" : "115804002",
        "display" : "En(a-)(Fin) phenotype"
      },
      {
        "code" : "115805001",
        "display" : "En(a-)(UK) phenotype"
      },
      {
        "code" : "115821006",
        "display" : "Lutheran blood group phenotype"
      },
      {
        "code" : "115822004",
        "display" : "Lutheran negative phenotype"
      },
      {
        "code" : "115823009",
        "display" : "LuLu phenotype"
      },
      {
        "code" : "115824003",
        "display" : "In(Lu) phenotype"
      },
      {
        "code" : "115825002",
        "display" : "XS2 phenotype"
      },
      {
        "code" : "115826001",
        "display" : "Acquired Lutheran negative phenotype"
      },
      {
        "code" : "115827005",
        "display" : "Lutheran weak phenotype"
      },
      {
        "code" : "115830003",
        "display" : "Kidd blood group phenotype"
      },
      {
        "code" : "115831004",
        "display" : "Jk(a-b-) phenotype"
      },
      {
        "code" : "115832006",
        "display" : "JkJk phenotype"
      },
      {
        "code" : "115833001",
        "display" : "In(Jk) phenotype"
      },
      {
        "code" : "115834007",
        "display" : "Duffy blood group phenotype"
      },
      {
        "code" : "115835008",
        "display" : "Fy(a-b-) phenotype"
      },
      {
        "code" : "115837000",
        "display" : "Kell blood group phenotype"
      },
      {
        "code" : "115838005",
        "display" : "Kell>null< phenotype"
      },
      {
        "code" : "115839002",
        "display" : "Kell>mod< phenotype"
      },
      {
        "code" : "115844009",
        "display" : "Kx blood group phenotype"
      },
      {
        "code" : "115845005",
        "display" : "McLeod phenotype"
      },
      {
        "code" : "115851000",
        "display" : "Colton blood group phenotype"
      },
      {
        "code" : "115852007",
        "display" : "Co(a-b-) phenotype"
      },
      {
        "code" : "115853002",
        "display" : "Gerbich blood group phenotype"
      },
      {
        "code" : "115854008",
        "display" : "Gerbich positive phenotype"
      },
      {
        "code" : "115855009",
        "display" : "Gerbich negative phenotype"
      },
      {
        "code" : "115860008",
        "display" : "Cromer blood group phenotype"
      },
      {
        "code" : "115861007",
        "display" : "Inab phenotype"
      },
      {
        "code" : "115866002",
        "display" : "Chido-Rodgers blood group phenotype"
      },
      {
        "code" : "115867006",
        "display" : "Ch-Rg- phenotype"
      },
      {
        "code" : "115940004",
        "display" : "Blood group phenotype"
      },
      {
        "code" : "1162254004",
        "display" : "Fetal blood group Rhesus negative"
      },
      {
        "code" : "1162255003",
        "display" : "Fetal blood group Rhesus positive"
      },
      {
        "code" : "131149001",
        "display" : "Blood group A>1<"
      },
      {
        "code" : "131150001",
        "display" : "Blood group A>2<"
      },
      {
        "code" : "131151002",
        "display" : "Blood group A>3<"
      },
      {
        "code" : "131152009",
        "display" : "Blood group A>x<"
      },
      {
        "code" : "131153004",
        "display" : "Blood group A>m<"
      },
      {
        "code" : "131154005",
        "display" : "Blood group A>y<"
      },
      {
        "code" : "131155006",
        "display" : "Blood group A>end<"
      },
      {
        "code" : "131156007",
        "display" : "Blood group A>el<"
      },
      {
        "code" : "131157003",
        "display" : "Blood group A variant"
      },
      {
        "code" : "131158008",
        "display" : "Blood group B variant"
      },
      {
        "code" : "131159000",
        "display" : "Blood group B>3<"
      },
      {
        "code" : "131160005",
        "display" : "Blood group B>m<"
      },
      {
        "code" : "131161009",
        "display" : "Blood group B>el<"
      },
      {
        "code" : "131162002",
        "display" : "Blood group B>w<"
      },
      {
        "code" : "131163007",
        "display" : "Blood group B>x<"
      },
      {
        "code" : "131164001",
        "display" : "Blood group A>m<^h^"
      },
      {
        "code" : "131165000",
        "display" : "Blood group B>m<^h^"
      },
      {
        "code" : "131166004",
        "display" : "Blood group O>m<^h^"
      },
      {
        "code" : "131167008",
        "display" : "Blood group O>Hm<"
      },
      {
        "code" : "131168003",
        "display" : "Blood group O>Hm<^A^"
      },
      {
        "code" : "131169006",
        "display" : "Blood group O>Hm<^B^"
      },
      {
        "code" : "131178000",
        "display" : "Gerbich type"
      },
      {
        "code" : "131179008",
        "display" : "Yus type"
      },
      {
        "code" : "131180006",
        "display" : "Melasian type"
      },
      {
        "code" : "131181005",
        "display" : "Leach type"
      },
      {
        "code" : "16345006",
        "display" : "Weak G phenotype"
      },
      {
        "code" : "165743006",
        "display" : "Blood group AB"
      },
      {
        "code" : "165746003",
        "display" : "RhD negative"
      },
      {
        "code" : "165747007",
        "display" : "RhD positive"
      },
      {
        "code" : "165751009",
        "display" : "Duffy blood group"
      },
      {
        "code" : "24403008",
        "display" : "p phenotype"
      },
      {
        "code" : "250376006",
        "display" : "Rh negative Du positive"
      },
      {
        "code" : "250389000",
        "display" : "Kell antigen type"
      },
      {
        "code" : "250390009",
        "display" : "Duffy antigen type"
      },
      {
        "code" : "250391008",
        "display" : "Kidd antigen type"
      },
      {
        "code" : "250392001",
        "display" : "MNS antigen type"
      },
      {
        "code" : "250394000",
        "display" : "Landsteiner-Weiner antigen type"
      },
      {
        "code" : "250395004",
        "display" : "Cartwright antigen type"
      },
      {
        "code" : "250396003",
        "display" : "Diego antigen type"
      },
      {
        "code" : "250397007",
        "display" : "Chido-Rogers antigen type"
      },
      {
        "code" : "250398002",
        "display" : "H antigen type"
      },
      {
        "code" : "250399005",
        "display" : "Kx antigen type"
      },
      {
        "code" : "250400003",
        "display" : "Low incidence antigen type"
      },
      {
        "code" : "25132006",
        "display" : "Weak N phenotype"
      },
      {
        "code" : "25384006",
        "display" : "Weak S phenotype"
      },
      {
        "code" : "278147001",
        "display" : "Blood group O Rh(D) positive"
      },
      {
        "code" : "278148006",
        "display" : "Blood group O Rh(D) negative"
      },
      {
        "code" : "278149003",
        "display" : "Blood group A Rh(D) positive"
      },
      {
        "code" : "278150003",
        "display" : "Blood group B Rh(D) positive"
      },
      {
        "code" : "278151004",
        "display" : "Blood group AB Rh(D) positive"
      },
      {
        "code" : "278152006",
        "display" : "Blood group A Rh(D) negative"
      },
      {
        "code" : "278153001",
        "display" : "Blood group B Rh(D) negative"
      },
      {
        "code" : "278154007",
        "display" : "Blood group AB Rh(D) negative"
      },
      {
        "code" : "3067005",
        "display" : "Weak C phenotype"
      },
      {
        "code" : "34850003",
        "display" : "Weak Fy^b^ phenotype"
      },
      {
        "code" : "365637002",
        "display" : "ABO blood group - finding"
      },
      {
        "code" : "365638007",
        "display" : "Finding of Rh (Rhesus) blood group"
      },
      {
        "code" : "365640002",
        "display" : "Common composite blood groups - finding"
      },
      {
        "code" : "365641003",
        "display" : "Minor blood groups - finding"
      },
      {
        "code" : "365642005",
        "display" : "Blood group antigen type - finding"
      },
      {
        "code" : "365643000",
        "display" : "Rh antigen type - finding"
      },
      {
        "code" : "365645007",
        "display" : "Finding of Rh (Rhesus) genotype"
      },
      {
        "code" : "38194003",
        "display" : "Weak e phenotype"
      },
      {
        "code" : "405847005",
        "display" : "Fy(a+b-) phenotype"
      },
      {
        "code" : "405848000",
        "display" : "Fy(a-b+) phenotype"
      },
      {
        "code" : "405849008",
        "display" : "Fy(a+b+) phenotype"
      },
      {
        "code" : "405850008",
        "display" : "Fy(a-) phenotype"
      },
      {
        "code" : "405851007",
        "display" : "Fy(a+) phenotype"
      },
      {
        "code" : "405852000",
        "display" : "Fy(b-) phenotype"
      },
      {
        "code" : "405853005",
        "display" : "Fy(b+) phenotype"
      },
      {
        "code" : "405854004",
        "display" : "Jk(a+) phenotype"
      },
      {
        "code" : "405855003",
        "display" : "Jk(a+b+) phenotype"
      },
      {
        "code" : "405856002",
        "display" : "Jk(a+b-) phenotype"
      },
      {
        "code" : "405857006",
        "display" : "Jk(a-) phenotype"
      },
      {
        "code" : "405858001",
        "display" : "Jk(a-b+) phenotype"
      },
      {
        "code" : "405859009",
        "display" : "Jk(b+) phenotype"
      },
      {
        "code" : "405860004",
        "display" : "Jk(b-) phenotype"
      },
      {
        "code" : "405861000",
        "display" : "Le(a+b-) phenotype"
      },
      {
        "code" : "405862007",
        "display" : "Le(a-b+) phenotype"
      },
      {
        "code" : "405863002",
        "display" : "Le(a-) phenotype"
      },
      {
        "code" : "405864008",
        "display" : "Le(a+) phenotype"
      },
      {
        "code" : "405865009",
        "display" : "Le(b+) phenotype"
      },
      {
        "code" : "405866005",
        "display" : "Le(b-) phenotype"
      },
      {
        "code" : "405868006",
        "display" : "Lu(a-b+) phenotype"
      },
      {
        "code" : "405869003",
        "display" : "Lu(a+b+) phenotype"
      },
      {
        "code" : "405870002",
        "display" : "Lu(a+b-) phenotype"
      },
      {
        "code" : "405871003",
        "display" : "Lu(a-) phenotype"
      },
      {
        "code" : "405872005",
        "display" : "Lu(a+) phenotype"
      },
      {
        "code" : "405873000",
        "display" : "Lu(b+) phenotype"
      },
      {
        "code" : "405874006",
        "display" : "Lu(b-) phenotype"
      },
      {
        "code" : "405875007",
        "display" : "M+ phenotype"
      },
      {
        "code" : "405876008",
        "display" : "M- phenotype"
      },
      {
        "code" : "405877004",
        "display" : "Le(a+b+) phenotype"
      },
      {
        "code" : "405878009",
        "display" : "N+ phenotype"
      },
      {
        "code" : "405879001",
        "display" : "N- phenotype"
      },
      {
        "code" : "405880003",
        "display" : "M-N- phenotype"
      },
      {
        "code" : "405881004",
        "display" : "M+N- phenotype"
      },
      {
        "code" : "405882006",
        "display" : "M+N+ phenotype"
      },
      {
        "code" : "405883001",
        "display" : "M-N+ phenotype"
      },
      {
        "code" : "405884007",
        "display" : "S- phenotype"
      },
      {
        "code" : "405885008",
        "display" : "S+ phenotype"
      },
      {
        "code" : "405886009",
        "display" : "s- phenotype"
      },
      {
        "code" : "405887000",
        "display" : "s+ phenotype"
      },
      {
        "code" : "405888005",
        "display" : "S+s+ phenotype"
      },
      {
        "code" : "405889002",
        "display" : "S-s+ phenotype"
      },
      {
        "code" : "405890006",
        "display" : "S-s- phenotype"
      },
      {
        "code" : "405891005",
        "display" : "S+s- phenotype"
      },
      {
        "code" : "405892003",
        "display" : "K+ phenotype"
      },
      {
        "code" : "405893008",
        "display" : "K- phenotype"
      },
      {
        "code" : "405894002",
        "display" : "k- phenotype"
      },
      {
        "code" : "405895001",
        "display" : "k+ phenotype"
      },
      {
        "code" : "405896000",
        "display" : "K+k+ phenotype"
      },
      {
        "code" : "405897009",
        "display" : "K+k- phenotype"
      },
      {
        "code" : "405898004",
        "display" : "K-k- phenotype"
      },
      {
        "code" : "405899007",
        "display" : "K-k+ phenotype"
      },
      {
        "code" : "405900002",
        "display" : "P1+ phenotype"
      },
      {
        "code" : "405901003",
        "display" : "P1- phenotype"
      },
      {
        "code" : "406002002",
        "display" : "cde haplotype"
      },
      {
        "code" : "406003007",
        "display" : "Cde haplotype"
      },
      {
        "code" : "406004001",
        "display" : "cdE haplotype"
      },
      {
        "code" : "406005000",
        "display" : "CDe haplotype"
      },
      {
        "code" : "406006004",
        "display" : "cDE haplotype"
      },
      {
        "code" : "406007008",
        "display" : "cDe haplotype"
      },
      {
        "code" : "406008003",
        "display" : "CdE haplotype"
      },
      {
        "code" : "406009006",
        "display" : "CDE haplotype"
      },
      {
        "code" : "45597001",
        "display" : "Blood group A>3<B"
      },
      {
        "code" : "57652005",
        "display" : "Weak V phenotype"
      },
      {
        "code" : "58460004",
        "display" : "Blood group O"
      },
      {
        "code" : "64553001",
        "display" : "Secretor gene absent (se)"
      },
      {
        "code" : "65087006",
        "display" : "Weak M phenotype"
      },
      {
        "code" : "6800004",
        "display" : "Weak E phenotype"
      },
      {
        "code" : "733119003",
        "display" : "Rhc negative"
      },
      {
        "code" : "733120009",
        "display" : "Rhc positive"
      },
      {
        "code" : "74836001",
        "display" : "Secretor gene present (Se)"
      },
      {
        "code" : "79248008",
        "display" : "Blood group A>1<B"
      },
      {
        "code" : "81835007",
        "display" : "Weak c phenotype"
      },
      {
        "code" : "88942003",
        "display" : "Blood group A>2<B"
      },
      {
        "code" : "89109006",
        "display" : "Weak D phenotype"
      }]
    }]
  }
}

```
