MyHealthEu MVC package - Local Development build (v9.1.0) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions
| Active as of 2026-02-19 |
@prefix fhir: <http://hl7.org/fhir/> . @prefix owl: <http://www.w3.org/2002/07/owl#> . @prefix rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> . @prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> . @prefix xsd: <http://www.w3.org/2001/XMLSchema#> . # - resource ------------------------------------------------------------------- a fhir:ValueSet ; fhir:nodeRole fhir:treeRoot ; fhir:id [ fhir:v "eHDSIBloodGroupLab"] ; # fhir:url [ fhir:v "http://terminology.ehdsi.eu/ValueSet/eHDSIBloodGroupLab"^^xsd:anyURI ; fhir:l <http://terminology.ehdsi.eu/ValueSet/eHDSIBloodGroupLab> ] ; # fhir:identifier ( [ fhir:system [ fhir:v "urn:ietf:rfc:3986"^^xsd:anyURI ; fhir:l <urn:ietf:rfc:3986> ] ; fhir:value [ fhir:v "urn:oid:1.3.6.1.4.1.12559.11.10.1.3.1.42.105" ] ] ) ; # fhir:version [ fhir:v "9.1.0"] ; # fhir:name [ fhir:v "EHDSIBloodGroupLab"] ; # fhir:title [ fhir:v "eHDSI Blood Group Laboratory"] ; # fhir:status [ fhir:v "active"] ; # fhir:experimental [ fhir:v false] ; # fhir:date [ fhir:v "2026-02-19T15:58:54+00:00"^^xsd:dateTime] ; # fhir:publisher [ fhir:v "MyHealth@Eu"] ; # fhir:contact ( [ fhir:name [ fhir:v "MyHealth@Eu" ] ; ( fhir:telecom [ fhir:system [ fhir:v "url" ] ; fhir:value [ fhir:v "https://health.ec.europa.eu/other-pages/basic-page/myhealtheu-flyer-addressed-patients-and-health-professionals_en" ] ] ) ] ) ; # fhir:description [ fhir:v "The Value Set is used to code the value of patient’s blood group + Rh."] ; # fhir:copyright [ fhir:v "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."] ; # fhir:compose [ ( fhir:include [ fhir:system [ fhir:v "http://snomed.info/sct"^^xsd:anyURI ; fhir:l <http://snomed.info/sct> ] ; ( fhir:concept [ fhir:code [ fhir:v "103225004" ] ; fhir:display [ fhir:v "P>2< phenotype" ] ] [ fhir:code [ fhir:v "112143006" ] ; fhir:display [ fhir:v "ABO group phenotype" ] ] [ fhir:code [ fhir:v "112144000" ] ; fhir:display [ fhir:v "Blood group A" ] ] [ fhir:code [ fhir:v "112149005" ] ; fhir:display [ fhir:v "Blood group B" ] ] [ fhir:code [ fhir:v "115730009" ] ; fhir:display [ fhir:v "Hh blood group phenotype" ] ] [ fhir:code [ fhir:v "115731008" ] ; fhir:display [ fhir:v "Blood group O>h< Bombay" ] ] [ fhir:code [ fhir:v "115732001" ] ; fhir:display [ fhir:v "Blood group O>h< Bombay Indian type" ] ] [ fhir:code [ fhir:v "115734000" ] ; fhir:display [ fhir:v "Blood group O>h< Bombay Reunion type" ] ] [ fhir:code [ fhir:v "115735004" ] ; fhir:display [ fhir:v "Blood group Para-Bombay" ] ] [ fhir:code [ fhir:v "115736003" ] ; fhir:display [ fhir:v "Blood group A>h<" ] ] [ fhir:code [ fhir:v "115737007" ] ; fhir:display [ fhir:v "Blood group B>h<" ] ] [ fhir:code [ fhir:v "115748000" ] ; fhir:display [ fhir:v "Lewis blood group phenotype" ] ] [ fhir:code [ fhir:v "115749008" ] ; fhir:display [ fhir:v "Le(a-b-) phenotype" ] ] [ fhir:code [ fhir:v "115750008" ] ; fhir:display [ fhir:v "I blood group phenotype" ] ] [ fhir:code [ fhir:v "115751007" ] ; fhir:display [ fhir:v "i>cord< phenotype" ] ] [ fhir:code [ fhir:v "115752000" ] ; fhir:display [ fhir:v "i>adult< phenotype" ] ] [ fhir:code [ fhir:v "115753005" ] ; fhir:display [ fhir:v "i>1< phenotype" ] ] [ fhir:code [ fhir:v "115754004" ] ; fhir:display [ fhir:v "i>2< phenotype" ] ] [ fhir:code [ fhir:v "115755003" ] ; fhir:display [ fhir:v "I phenotype" ] ] [ fhir:code [ fhir:v "115756002" ] ; fhir:display [ fhir:v "I>int< phenotype" ] ] [ fhir:code [ fhir:v "115758001" ] ; fhir:display [ fhir:v "Rh (Rhesus) blood group phenotype" ] ] [ fhir:code [ fhir:v "115759009" ] ; fhir:display [ fhir:v "Rh>null< phenotype" ] ] [ fhir:code [ fhir:v "115760004" ] ; fhir:display [ fhir:v "X^o^rX^o^r blood group phenotype" ] ] [ fhir:code [ fhir:v "115761000" ] ; fhir:display [ fhir:v "Rr^-^ blood group phenotype" ] ] [ fhir:code [ fhir:v "115762007" ] ; fhir:display [ fhir:v "Rh>mod< blood group phenotype" ] ] [ fhir:code [ fhir:v "115763002" ] ; fhir:display [ fhir:v "Trans weak D phenotype" ] ] [ fhir:code [ fhir:v "115764008" ] ; fhir:display [ fhir:v "Inherited weak D phenotype" ] ] [ fhir:code [ fhir:v "115794002" ] ; fhir:display [ fhir:v "P blood group phenotype" ] ] [ fhir:code [ fhir:v "115795001" ] ; fhir:display [ fhir:v "P>1< phenotype" ] ] [ fhir:code [ fhir:v "115796000" ] ; fhir:display [ fhir:v "P>1<^k^ phenotype" ] ] [ fhir:code [ fhir:v "115797009" ] ; fhir:display [ fhir:v "P>2<^k^ phenotype" ] ] [ fhir:code [ fhir:v "115798004" ] ; fhir:display [ fhir:v "Landsteiner-Wiener phenotype" ] ] [ fhir:code [ fhir:v "115799007" ] ; fhir:display [ fhir:v "LW(a-b-) phenotype" ] ] [ fhir:code [ fhir:v "115800006" ] ; fhir:display [ fhir:v "MNS blood group phenotype" ] ] [ fhir:code [ fhir:v "115801005" ] ; fhir:display [ fhir:v "M^k^M^k^ phenotype" ] ] [ fhir:code [ fhir:v "115802003" ] ; fhir:display [ fhir:v "U- phenotype" ] ] [ fhir:code [ fhir:v "115803008" ] ; fhir:display [ fhir:v "En(a-) phenotype" ] ] [ fhir:code [ fhir:v "115804002" ] ; fhir:display [ fhir:v "En(a-)(Fin) phenotype" ] ] [ fhir:code [ fhir:v "115805001" ] ; fhir:display [ fhir:v "En(a-)(UK) phenotype" ] ] [ fhir:code [ fhir:v "115821006" ] ; fhir:display [ fhir:v "Lutheran blood group phenotype" ] ] [ fhir:code [ fhir:v "115822004" ] ; fhir:display [ fhir:v "Lutheran negative phenotype" ] ] [ fhir:code [ fhir:v "115823009" ] ; fhir:display [ fhir:v "LuLu phenotype" ] ] [ fhir:code [ fhir:v "115824003" ] ; fhir:display [ fhir:v "In(Lu) phenotype" ] ] [ fhir:code [ fhir:v "115825002" ] ; fhir:display [ fhir:v "XS2 phenotype" ] ] [ fhir:code [ fhir:v "115826001" ] ; fhir:display [ fhir:v "Acquired Lutheran negative phenotype" ] ] [ fhir:code [ fhir:v "115827005" ] ; fhir:display [ fhir:v "Lutheran weak phenotype" ] ] [ fhir:code [ fhir:v "115830003" ] ; fhir:display [ fhir:v "Kidd blood group phenotype" ] ] [ fhir:code [ fhir:v "115831004" ] ; fhir:display [ fhir:v "Jk(a-b-) phenotype" ] ] [ fhir:code [ fhir:v "115832006" ] ; fhir:display [ fhir:v "JkJk phenotype" ] ] [ fhir:code [ fhir:v "115833001" ] ; fhir:display [ fhir:v "In(Jk) phenotype" ] ] [ fhir:code [ fhir:v "115834007" ] ; fhir:display [ fhir:v "Duffy blood group phenotype" ] ] [ fhir:code [ fhir:v "115835008" ] ; fhir:display [ fhir:v "Fy(a-b-) phenotype" ] ] [ fhir:code [ fhir:v "115837000" ] ; fhir:display [ fhir:v "Kell blood group phenotype" ] ] [ fhir:code [ fhir:v "115838005" ] ; fhir:display [ fhir:v "Kell>null< phenotype" ] ] [ fhir:code [ fhir:v "115839002" ] ; fhir:display [ fhir:v "Kell>mod< phenotype" ] ] [ fhir:code [ fhir:v "115844009" ] ; fhir:display [ fhir:v "Kx blood group phenotype" ] ] [ fhir:code [ fhir:v "115845005" ] ; fhir:display [ fhir:v "McLeod phenotype" ] ] [ fhir:code [ fhir:v "115851000" ] ; fhir:display [ fhir:v "Colton blood group phenotype" ] ] [ fhir:code [ fhir:v "115852007" ] ; fhir:display [ fhir:v "Co(a-b-) phenotype" ] ] [ fhir:code [ fhir:v "115853002" ] ; fhir:display [ fhir:v "Gerbich blood group phenotype" ] ] [ fhir:code [ fhir:v "115854008" ] ; fhir:display [ fhir:v "Gerbich positive phenotype" ] ] [ fhir:code [ fhir:v "115855009" ] ; fhir:display [ fhir:v "Gerbich negative phenotype" ] ] [ fhir:code [ fhir:v "115860008" ] ; fhir:display [ fhir:v "Cromer blood group phenotype" ] ] [ fhir:code [ fhir:v "115861007" ] ; fhir:display [ fhir:v "Inab phenotype" ] ] [ fhir:code [ fhir:v "115866002" ] ; fhir:display [ fhir:v "Chido-Rodgers blood group phenotype" ] ] [ fhir:code [ fhir:v "115867006" ] ; fhir:display [ fhir:v "Ch-Rg- phenotype" ] ] [ fhir:code [ fhir:v "115940004" ] ; fhir:display [ fhir:v "Blood group phenotype" ] ] [ fhir:code [ fhir:v "1162254004" ] ; fhir:display [ fhir:v "Fetal blood group Rhesus negative" ] ] [ fhir:code [ fhir:v "1162255003" ] ; fhir:display [ fhir:v "Fetal blood group Rhesus positive" ] ] [ fhir:code [ fhir:v "131149001" ] ; fhir:display [ fhir:v "Blood group A>1<" ] ] [ fhir:code [ fhir:v "131150001" ] ; fhir:display [ fhir:v "Blood group A>2<" ] ] [ fhir:code [ fhir:v "131151002" ] ; fhir:display [ fhir:v "Blood group A>3<" ] ] [ fhir:code [ fhir:v "131152009" ] ; fhir:display [ fhir:v "Blood group A>x<" ] ] [ fhir:code [ fhir:v "131153004" ] ; fhir:display [ fhir:v "Blood group A>m<" ] ] [ fhir:code [ fhir:v "131154005" ] ; fhir:display [ fhir:v "Blood group A>y<" ] ] [ fhir:code [ fhir:v "131155006" ] ; fhir:display [ fhir:v "Blood group A>end<" ] ] [ fhir:code [ fhir:v "131156007" ] ; fhir:display [ fhir:v "Blood group A>el<" ] ] [ fhir:code [ fhir:v "131157003" ] ; fhir:display [ fhir:v "Blood group A variant" ] ] [ fhir:code [ fhir:v "131158008" ] ; fhir:display [ fhir:v "Blood group B variant" ] ] [ fhir:code [ fhir:v "131159000" ] ; fhir:display [ fhir:v "Blood group B>3<" ] ] [ fhir:code [ fhir:v "131160005" ] ; fhir:display [ fhir:v "Blood group B>m<" ] ] [ fhir:code [ fhir:v "131161009" ] ; fhir:display [ fhir:v "Blood group B>el<" ] ] [ fhir:code [ fhir:v "131162002" ] ; fhir:display [ fhir:v "Blood group B>w<" ] ] [ fhir:code [ fhir:v "131163007" ] ; fhir:display [ fhir:v "Blood group B>x<" ] ] [ fhir:code [ fhir:v "131164001" ] ; fhir:display [ fhir:v "Blood group A>m<^h^" ] ] [ fhir:code [ fhir:v "131165000" ] ; fhir:display [ fhir:v "Blood group B>m<^h^" ] ] [ fhir:code [ fhir:v "131166004" ] ; fhir:display [ fhir:v "Blood group O>m<^h^" ] ] [ fhir:code [ fhir:v "131167008" ] ; fhir:display [ fhir:v "Blood group O>Hm<" ] ] [ fhir:code [ fhir:v "131168003" ] ; fhir:display [ fhir:v "Blood group O>Hm<^A^" ] ] [ fhir:code [ fhir:v "131169006" ] ; fhir:display [ fhir:v "Blood group O>Hm<^B^" ] ] [ fhir:code [ fhir:v "131178000" ] ; fhir:display [ fhir:v "Gerbich type" ] ] [ fhir:code [ fhir:v "131179008" ] ; fhir:display [ fhir:v "Yus type" ] ] [ fhir:code [ fhir:v "131180006" ] ; fhir:display [ fhir:v "Melasian type" ] ] [ fhir:code [ fhir:v "131181005" ] ; fhir:display [ fhir:v "Leach type" ] ] [ fhir:code [ fhir:v "16345006" ] ; fhir:display [ fhir:v "Weak G phenotype" ] ] [ fhir:code [ fhir:v "165743006" ] ; fhir:display [ fhir:v "Blood group AB" ] ] [ fhir:code [ fhir:v "165746003" ] ; fhir:display [ fhir:v "RhD negative" ] ] [ fhir:code [ fhir:v "165747007" ] ; fhir:display [ fhir:v "RhD positive" ] ] [ fhir:code [ fhir:v "165751009" ] ; fhir:display [ fhir:v "Duffy blood group" ] ] [ fhir:code [ fhir:v "24403008" ] ; fhir:display [ fhir:v "p phenotype" ] ] [ fhir:code [ fhir:v "250376006" ] ; fhir:display [ fhir:v "Rh negative Du positive" ] ] [ fhir:code [ fhir:v "250389000" ] ; fhir:display [ fhir:v "Kell antigen type" ] ] [ fhir:code [ fhir:v "250390009" ] ; fhir:display [ fhir:v "Duffy antigen type" ] ] [ fhir:code [ fhir:v "250391008" ] ; fhir:display [ fhir:v "Kidd antigen type" ] ] [ fhir:code [ fhir:v "250392001" ] ; fhir:display [ fhir:v "MNS antigen type" ] ] [ fhir:code [ fhir:v "250394000" ] ; fhir:display [ fhir:v "Landsteiner-Weiner antigen type" ] ] [ fhir:code [ fhir:v "250395004" ] ; fhir:display [ fhir:v "Cartwright antigen type" ] ] [ fhir:code [ fhir:v "250396003" ] ; fhir:display [ fhir:v "Diego antigen type" ] ] [ fhir:code [ fhir:v "250397007" ] ; fhir:display [ fhir:v "Chido-Rogers antigen type" ] ] [ fhir:code [ fhir:v "250398002" ] ; fhir:display [ fhir:v "H antigen type" ] ] [ fhir:code [ fhir:v "250399005" ] ; fhir:display [ fhir:v "Kx antigen type" ] ] [ fhir:code [ fhir:v "250400003" ] ; fhir:display [ fhir:v "Low incidence antigen type" ] ] [ fhir:code [ fhir:v "25132006" ] ; fhir:display [ fhir:v "Weak N phenotype" ] ] [ fhir:code [ fhir:v "25384006" ] ; fhir:display [ fhir:v "Weak S phenotype" ] ] [ fhir:code [ fhir:v "278147001" ] ; fhir:display [ fhir:v "Blood group O Rh(D) positive" ] ] [ fhir:code [ fhir:v "278148006" ] ; fhir:display [ fhir:v "Blood group O Rh(D) negative" ] ] [ fhir:code [ fhir:v "278149003" ] ; fhir:display [ fhir:v "Blood group A Rh(D) positive" ] ] [ fhir:code [ fhir:v "278150003" ] ; fhir:display [ fhir:v "Blood group B Rh(D) positive" ] ] [ fhir:code [ fhir:v "278151004" ] ; fhir:display [ fhir:v "Blood group AB Rh(D) positive" ] ] [ fhir:code [ fhir:v "278152006" ] ; fhir:display [ fhir:v "Blood group A Rh(D) negative" ] ] [ fhir:code [ fhir:v "278153001" ] ; fhir:display [ fhir:v "Blood group B Rh(D) negative" ] ] [ fhir:code [ fhir:v "278154007" ] ; fhir:display [ fhir:v "Blood group AB Rh(D) negative" ] ] [ fhir:code [ fhir:v "3067005" ] ; fhir:display [ fhir:v "Weak C phenotype" ] ] [ fhir:code [ fhir:v "34850003" ] ; fhir:display [ fhir:v "Weak Fy^b^ phenotype" ] ] [ fhir:code [ fhir:v "365637002" ] ; fhir:display [ fhir:v "ABO blood group - finding" ] ] [ fhir:code [ fhir:v "365638007" ] ; fhir:display [ fhir:v "Finding of Rh (Rhesus) blood group" ] ] [ fhir:code [ fhir:v "365640002" ] ; fhir:display [ fhir:v "Common composite blood groups - finding" ] ] [ fhir:code [ fhir:v "365641003" ] ; fhir:display [ fhir:v "Minor blood groups - finding" ] ] [ fhir:code [ fhir:v "365642005" ] ; fhir:display [ fhir:v "Blood group antigen type - finding" ] ] [ fhir:code [ fhir:v "365643000" ] ; fhir:display [ fhir:v "Rh antigen type - finding" ] ] [ fhir:code [ fhir:v "365645007" ] ; fhir:display [ fhir:v "Finding of Rh (Rhesus) genotype" ] ] [ fhir:code [ fhir:v "38194003" ] ; fhir:display [ fhir:v "Weak e phenotype" ] ] [ fhir:code [ fhir:v "405847005" ] ; fhir:display [ fhir:v "Fy(a+b-) phenotype" ] ] [ fhir:code [ fhir:v "405848000" ] ; fhir:display [ fhir:v "Fy(a-b+) phenotype" ] ] [ fhir:code [ fhir:v "405849008" ] ; fhir:display [ fhir:v "Fy(a+b+) phenotype" ] ] [ fhir:code [ fhir:v "405850008" ] ; fhir:display [ fhir:v "Fy(a-) phenotype" ] ] [ fhir:code [ fhir:v "405851007" ] ; fhir:display [ fhir:v "Fy(a+) phenotype" ] ] [ fhir:code [ fhir:v "405852000" ] ; fhir:display [ fhir:v "Fy(b-) phenotype" ] ] [ fhir:code [ fhir:v "405853005" ] ; fhir:display [ fhir:v "Fy(b+) phenotype" ] ] [ fhir:code [ fhir:v "405854004" ] ; fhir:display [ fhir:v "Jk(a+) phenotype" ] ] [ fhir:code [ fhir:v "405855003" ] ; fhir:display [ fhir:v "Jk(a+b+) phenotype" ] ] [ fhir:code [ fhir:v "405856002" ] ; fhir:display [ fhir:v "Jk(a+b-) phenotype" ] ] [ fhir:code [ fhir:v "405857006" ] ; fhir:display [ fhir:v "Jk(a-) phenotype" ] ] [ fhir:code [ fhir:v "405858001" ] ; fhir:display [ fhir:v "Jk(a-b+) phenotype" ] ] [ fhir:code [ fhir:v "405859009" ] ; fhir:display [ fhir:v "Jk(b+) phenotype" ] ] [ fhir:code [ fhir:v "405860004" ] ; fhir:display [ fhir:v "Jk(b-) phenotype" ] ] [ fhir:code [ fhir:v "405861000" ] ; fhir:display [ fhir:v "Le(a+b-) phenotype" ] ] [ fhir:code [ fhir:v "405862007" ] ; fhir:display [ fhir:v "Le(a-b+) phenotype" ] ] [ fhir:code [ fhir:v "405863002" ] ; fhir:display [ fhir:v "Le(a-) phenotype" ] ] [ fhir:code [ fhir:v "405864008" ] ; fhir:display [ fhir:v "Le(a+) phenotype" ] ] [ fhir:code [ fhir:v "405865009" ] ; fhir:display [ fhir:v "Le(b+) phenotype" ] ] [ fhir:code [ fhir:v "405866005" ] ; fhir:display [ fhir:v "Le(b-) phenotype" ] ] [ fhir:code [ fhir:v "405868006" ] ; fhir:display [ fhir:v "Lu(a-b+) phenotype" ] ] [ fhir:code [ fhir:v "405869003" ] ; fhir:display [ fhir:v "Lu(a+b+) phenotype" ] ] [ fhir:code [ fhir:v "405870002" ] ; fhir:display [ fhir:v "Lu(a+b-) phenotype" ] ] [ fhir:code [ fhir:v "405871003" ] ; fhir:display [ fhir:v "Lu(a-) phenotype" ] ] [ fhir:code [ fhir:v "405872005" ] ; fhir:display [ fhir:v "Lu(a+) phenotype" ] ] [ fhir:code [ fhir:v "405873000" ] ; fhir:display [ fhir:v "Lu(b+) phenotype" ] ] [ fhir:code [ fhir:v "405874006" ] ; fhir:display [ fhir:v "Lu(b-) phenotype" ] ] [ fhir:code [ fhir:v "405875007" ] ; fhir:display [ fhir:v "M+ phenotype" ] ] [ fhir:code [ fhir:v "405876008" ] ; fhir:display [ fhir:v "M- phenotype" ] ] [ fhir:code [ fhir:v "405877004" ] ; fhir:display [ fhir:v "Le(a+b+) phenotype" ] ] [ fhir:code [ fhir:v "405878009" ] ; fhir:display [ fhir:v "N+ phenotype" ] ] [ fhir:code [ fhir:v "405879001" ] ; fhir:display [ fhir:v "N- phenotype" ] ] [ fhir:code [ fhir:v "405880003" ] ; fhir:display [ fhir:v "M-N- phenotype" ] ] [ fhir:code [ fhir:v "405881004" ] ; fhir:display [ fhir:v "M+N- phenotype" ] ] [ fhir:code [ fhir:v "405882006" ] ; fhir:display [ fhir:v "M+N+ phenotype" ] ] [ fhir:code [ fhir:v "405883001" ] ; fhir:display [ fhir:v "M-N+ phenotype" ] ] [ fhir:code [ fhir:v "405884007" ] ; fhir:display [ fhir:v "S- phenotype" ] ] [ fhir:code [ fhir:v "405885008" ] ; fhir:display [ fhir:v "S+ phenotype" ] ] [ fhir:code [ fhir:v "405886009" ] ; fhir:display [ fhir:v "s- phenotype" ] ] [ fhir:code [ fhir:v "405887000" ] ; fhir:display [ fhir:v "s+ phenotype" ] ] [ fhir:code [ fhir:v "405888005" ] ; fhir:display [ fhir:v "S+s+ phenotype" ] ] [ fhir:code [ fhir:v "405889002" ] ; fhir:display [ fhir:v "S-s+ phenotype" ] ] [ fhir:code [ fhir:v "405890006" ] ; fhir:display [ fhir:v "S-s- phenotype" ] ] [ fhir:code [ fhir:v "405891005" ] ; fhir:display [ fhir:v "S+s- phenotype" ] ] [ fhir:code [ fhir:v "405892003" ] ; fhir:display [ fhir:v "K+ phenotype" ] ] [ fhir:code [ fhir:v "405893008" ] ; fhir:display [ fhir:v "K- phenotype" ] ] [ fhir:code [ fhir:v "405894002" ] ; fhir:display [ fhir:v "k- phenotype" ] ] [ fhir:code [ fhir:v "405895001" ] ; fhir:display [ fhir:v "k+ phenotype" ] ] [ fhir:code [ fhir:v "405896000" ] ; fhir:display [ fhir:v "K+k+ phenotype" ] ] [ fhir:code [ fhir:v "405897009" ] ; fhir:display [ fhir:v "K+k- phenotype" ] ] [ fhir:code [ fhir:v "405898004" ] ; fhir:display [ fhir:v "K-k- phenotype" ] ] [ fhir:code [ fhir:v "405899007" ] ; fhir:display [ fhir:v "K-k+ phenotype" ] ] [ fhir:code [ fhir:v "405900002" ] ; fhir:display [ fhir:v "P1+ phenotype" ] ] [ fhir:code [ fhir:v "405901003" ] ; fhir:display [ fhir:v "P1- phenotype" ] ] [ fhir:code [ fhir:v "406002002" ] ; fhir:display [ fhir:v "cde haplotype" ] ] [ fhir:code [ fhir:v "406003007" ] ; fhir:display [ fhir:v "Cde haplotype" ] ] [ fhir:code [ fhir:v "406004001" ] ; fhir:display [ fhir:v "cdE haplotype" ] ] [ fhir:code [ fhir:v "406005000" ] ; fhir:display [ fhir:v "CDe haplotype" ] ] [ fhir:code [ fhir:v "406006004" ] ; fhir:display [ fhir:v "cDE haplotype" ] ] [ fhir:code [ fhir:v "406007008" ] ; fhir:display [ fhir:v "cDe haplotype" ] ] [ fhir:code [ fhir:v "406008003" ] ; fhir:display [ fhir:v "CdE haplotype" ] ] [ fhir:code [ fhir:v "406009006" ] ; fhir:display [ fhir:v "CDE haplotype" ] ] [ fhir:code [ fhir:v "45597001" ] ; fhir:display [ fhir:v "Blood group A>3<B" ] ] [ fhir:code [ fhir:v "57652005" ] ; fhir:display [ fhir:v "Weak V phenotype" ] ] [ fhir:code [ fhir:v "58460004" ] ; fhir:display [ fhir:v "Blood group O" ] ] [ fhir:code [ fhir:v "64553001" ] ; fhir:display [ fhir:v "Secretor gene absent (se)" ] ] [ fhir:code [ fhir:v "65087006" ] ; fhir:display [ fhir:v "Weak M phenotype" ] ] [ fhir:code [ fhir:v "6800004" ] ; fhir:display [ fhir:v "Weak E phenotype" ] ] [ fhir:code [ fhir:v "733119003" ] ; fhir:display [ fhir:v "Rhc negative" ] ] [ fhir:code [ fhir:v "733120009" ] ; fhir:display [ fhir:v "Rhc positive" ] ] [ fhir:code [ fhir:v "74836001" ] ; fhir:display [ fhir:v "Secretor gene present (Se)" ] ] [ fhir:code [ fhir:v "79248008" ] ; fhir:display [ fhir:v "Blood group A>1<B" ] ] [ fhir:code [ fhir:v "81835007" ] ; fhir:display [ fhir:v "Weak c phenotype" ] ] [ fhir:code [ fhir:v "88942003" ] ; fhir:display [ fhir:v "Blood group A>2<B" ] ] [ fhir:code [ fhir:v "89109006" ] ; fhir:display [ fhir:v "Weak D phenotype" ] ] ) ] ) ] . #
IG © 2023+ MyHealth@Eu. Package myhealth.eu.fhir.mvc-package#9.1.0 based on FHIR 4.0.1. Generated 2026-02-19