FHIR IG analytics
| Package | myhealth.eu.fhir.mvc-package |
| Resource Type | ValueSet |
| Id | ValueSet-eHDSIBloodGroupLab.json |
| FHIR Version | R4 |
| Source | http://fhir.ehdsi.eu/mvc-package/9.1.0/ValueSet-eHDSIBloodGroupLab.html |
| URL | http://terminology.ehdsi.eu/ValueSet/eHDSIBloodGroupLab |
| Version | 9.1.0 |
| Status | active |
| Date | 2026-05-08T11:21:08+02:00 |
| Name | EHDSIBloodGroupLab |
| Title | eHDSI Blood Group Laboratory |
| 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. |
Resources that use this resource
Resources that this resource uses
| CodeSystem |
| hl7.fhir.vn.core#current | sct | SNOMED CT (all versions) |
Narrative
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Source1
{
"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"
}
]
}
]
}
}
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