MyHealth@Eu Laboratory Report
0.1.1 - trial-use
150
MyHealth@Eu Laboratory Report
0.1.1 - trial-use
150
MyHealth@Eu Laboratory Report - Local Development build (v0.1.1) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions
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@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:text [ fhir:status [ fhir:v "generated" ] ; fhir:div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: ValueSet eHDSIBloodGroupLab</b></p><a name=\"eHDSIBloodGroupLab\"> </a><a name=\"hceHDSIBloodGroupLab\"> </a><a name=\"eHDSIBloodGroupLab-en-US\"> </a><ul><li>Include these codes as defined in <a href=\"http://www.snomed.org/\"><code>http://snomed.info/sct</code></a><table class=\"none\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td><a href=\"http://snomed.info/id/1162255003\">1162255003</a></td><td>Fetal blood group Rhesus positive</td></tr><tr><td><a href=\"http://snomed.info/id/1162254004\">1162254004</a></td><td>Fetal blood group Rhesus negative</td></tr><tr><td><a href=\"http://snomed.info/id/733120009\">733120009</a></td><td>Rhc positive</td></tr><tr><td><a href=\"http://snomed.info/id/733119003\">733119003</a></td><td>Rhc negative</td></tr><tr><td><a href=\"http://snomed.info/id/406009006\">406009006</a></td><td>CDE haplotype</td></tr><tr><td><a href=\"http://snomed.info/id/406008003\">406008003</a></td><td>CdE haplotype</td></tr><tr><td><a href=\"http://snomed.info/id/406007008\">406007008</a></td><td>cDe haplotype</td></tr><tr><td><a href=\"http://snomed.info/id/406006004\">406006004</a></td><td>cDE haplotype</td></tr><tr><td><a href=\"http://snomed.info/id/406005000\">406005000</a></td><td>CDe haplotype</td></tr><tr><td><a href=\"http://snomed.info/id/406004001\">406004001</a></td><td>cdE haplotype</td></tr><tr><td><a href=\"http://snomed.info/id/406003007\">406003007</a></td><td>Cde haplotype</td></tr><tr><td><a href=\"http://snomed.info/id/406002002\">406002002</a></td><td>cde haplotype</td></tr><tr><td><a href=\"http://snomed.info/id/405901003\">405901003</a></td><td>P1- phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405900002\">405900002</a></td><td>P1+ phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405899007\">405899007</a></td><td>K-k+ phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405898004\">405898004</a></td><td>K-k- phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405897009\">405897009</a></td><td>K+k- phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405896000\">405896000</a></td><td>K+k+ phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405895001\">405895001</a></td><td>k+ phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405894002\">405894002</a></td><td>k- phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405893008\">405893008</a></td><td>K- phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405892003\">405892003</a></td><td>K+ phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405891005\">405891005</a></td><td>S+s- phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405890006\">405890006</a></td><td>S-s- phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405889002\">405889002</a></td><td>S-s+ phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405888005\">405888005</a></td><td>S+s+ phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405887000\">405887000</a></td><td>s+ phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405886009\">405886009</a></td><td>s- phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405885008\">405885008</a></td><td>S+ phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405884007\">405884007</a></td><td>S- phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405883001\">405883001</a></td><td>M-N+ phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405882006\">405882006</a></td><td>M+N+ phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405881004\">405881004</a></td><td>M+N- phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405880003\">405880003</a></td><td>M-N- phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405879001\">405879001</a></td><td>N- phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405878009\">405878009</a></td><td>N+ phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405877004\">405877004</a></td><td>Le(a+b+) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405876008\">405876008</a></td><td>M- phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405875007\">405875007</a></td><td>M+ phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405874006\">405874006</a></td><td>Lu(b-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405873000\">405873000</a></td><td>Lu(b+) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405872005\">405872005</a></td><td>Lu(a+) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405871003\">405871003</a></td><td>Lu(a-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405870002\">405870002</a></td><td>Lu(a+b-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405869003\">405869003</a></td><td>Lu(a+b+) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405868006\">405868006</a></td><td>Lu(a-b+) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405866005\">405866005</a></td><td>Le(b-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405865009\">405865009</a></td><td>Le(b+) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405864008\">405864008</a></td><td>Le(a+) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405863002\">405863002</a></td><td>Le(a-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405862007\">405862007</a></td><td>Le(a-b+) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405861000\">405861000</a></td><td>Le(a+b-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405860004\">405860004</a></td><td>Jk(b-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405859009\">405859009</a></td><td>Jk(b+) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405858001\">405858001</a></td><td>Jk(a-b+) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405857006\">405857006</a></td><td>Jk(a-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405856002\">405856002</a></td><td>Jk(a+b-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405855003\">405855003</a></td><td>Jk(a+b+) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405854004\">405854004</a></td><td>Jk(a+) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405853005\">405853005</a></td><td>Fy(b+) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405852000\">405852000</a></td><td>Fy(b-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405851007\">405851007</a></td><td>Fy(a+) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405850008\">405850008</a></td><td>Fy(a-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405849008\">405849008</a></td><td>Fy(a+b+) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405848000\">405848000</a></td><td>Fy(a-b+) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/405847005\">405847005</a></td><td>Fy(a+b-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/365645007\">365645007</a></td><td>Finding of Rh (Rhesus) genotype</td></tr><tr><td><a href=\"http://snomed.info/id/365643000\">365643000</a></td><td>Rh antigen type - finding</td></tr><tr><td><a href=\"http://snomed.info/id/365642005\">365642005</a></td><td>Blood group antigen type - finding</td></tr><tr><td><a href=\"http://snomed.info/id/365641003\">365641003</a></td><td>Minor blood groups - finding</td></tr><tr><td><a href=\"http://snomed.info/id/365640002\">365640002</a></td><td>Common composite blood groups - finding</td></tr><tr><td><a href=\"http://snomed.info/id/365638007\">365638007</a></td><td>Finding of Rh (Rhesus) blood group</td></tr><tr><td><a href=\"http://snomed.info/id/365637002\">365637002</a></td><td>ABO blood group - finding</td></tr><tr><td><a href=\"http://snomed.info/id/278154007\">278154007</a></td><td>Blood group AB Rh(D) negative</td></tr><tr><td><a href=\"http://snomed.info/id/278153001\">278153001</a></td><td>Blood group B Rh(D) negative</td></tr><tr><td><a href=\"http://snomed.info/id/278152006\">278152006</a></td><td>Blood group A Rh(D) negative</td></tr><tr><td><a href=\"http://snomed.info/id/278151004\">278151004</a></td><td>Blood group AB Rh(D) positive</td></tr><tr><td><a href=\"http://snomed.info/id/278150003\">278150003</a></td><td>Blood group B Rh(D) positive</td></tr><tr><td><a href=\"http://snomed.info/id/278149003\">278149003</a></td><td>Blood group A Rh(D) positive</td></tr><tr><td><a href=\"http://snomed.info/id/278148006\">278148006</a></td><td>Blood group O Rh(D) negative</td></tr><tr><td><a href=\"http://snomed.info/id/278147001\">278147001</a></td><td>Blood group O Rh(D) positive</td></tr><tr><td><a href=\"http://snomed.info/id/250400003\">250400003</a></td><td>Low incidence antigen type</td></tr><tr><td><a href=\"http://snomed.info/id/250399005\">250399005</a></td><td>Kx antigen type</td></tr><tr><td><a href=\"http://snomed.info/id/250398002\">250398002</a></td><td>H antigen type</td></tr><tr><td><a href=\"http://snomed.info/id/250397007\">250397007</a></td><td>Chido-Rogers antigen type</td></tr><tr><td><a href=\"http://snomed.info/id/250396003\">250396003</a></td><td>Diego antigen type</td></tr><tr><td><a href=\"http://snomed.info/id/250395004\">250395004</a></td><td>Cartwright antigen type</td></tr><tr><td><a href=\"http://snomed.info/id/250394000\">250394000</a></td><td>Landsteiner-Weiner antigen type</td></tr><tr><td><a href=\"http://snomed.info/id/250392001\">250392001</a></td><td>MNS antigen type</td></tr><tr><td><a href=\"http://snomed.info/id/250391008\">250391008</a></td><td>Kidd antigen type</td></tr><tr><td><a href=\"http://snomed.info/id/250390009\">250390009</a></td><td>Duffy antigen type</td></tr><tr><td><a href=\"http://snomed.info/id/250389000\">250389000</a></td><td>Kell antigen type</td></tr><tr><td><a href=\"http://snomed.info/id/250376006\">250376006</a></td><td>Rh negative Du positive</td></tr><tr><td><a href=\"http://snomed.info/id/165751009\">165751009</a></td><td>Duffy blood group</td></tr><tr><td><a href=\"http://snomed.info/id/165747007\">165747007</a></td><td>RhD positive</td></tr><tr><td><a href=\"http://snomed.info/id/165746003\">165746003</a></td><td>RhD negative</td></tr><tr><td><a href=\"http://snomed.info/id/165743006\">165743006</a></td><td>Blood group AB</td></tr><tr><td><a href=\"http://snomed.info/id/131181005\">131181005</a></td><td>Leach type</td></tr><tr><td><a href=\"http://snomed.info/id/131180006\">131180006</a></td><td>Melasian type</td></tr><tr><td><a href=\"http://snomed.info/id/131179008\">131179008</a></td><td>Yus type</td></tr><tr><td><a href=\"http://snomed.info/id/131178000\">131178000</a></td><td>Gerbich type</td></tr><tr><td><a href=\"http://snomed.info/id/131169006\">131169006</a></td><td>Blood group O>Hm<^B^</td></tr><tr><td><a href=\"http://snomed.info/id/131168003\">131168003</a></td><td>Blood group O>Hm<^A^</td></tr><tr><td><a href=\"http://snomed.info/id/131167008\">131167008</a></td><td>Blood group O>Hm<</td></tr><tr><td><a href=\"http://snomed.info/id/131166004\">131166004</a></td><td>Blood group O>m<^h^</td></tr><tr><td><a href=\"http://snomed.info/id/131165000\">131165000</a></td><td>Blood group B>m<^h^</td></tr><tr><td><a href=\"http://snomed.info/id/131164001\">131164001</a></td><td>Blood group A>m<^h^</td></tr><tr><td><a href=\"http://snomed.info/id/131163007\">131163007</a></td><td>Blood group B>x<</td></tr><tr><td><a href=\"http://snomed.info/id/131162002\">131162002</a></td><td>Blood group B>w<</td></tr><tr><td><a href=\"http://snomed.info/id/131161009\">131161009</a></td><td>Blood group B>el<</td></tr><tr><td><a href=\"http://snomed.info/id/131160005\">131160005</a></td><td>Blood group B>m<</td></tr><tr><td><a href=\"http://snomed.info/id/131159000\">131159000</a></td><td>Blood group B>3<</td></tr><tr><td><a href=\"http://snomed.info/id/131158008\">131158008</a></td><td>Blood group B variant</td></tr><tr><td><a href=\"http://snomed.info/id/131157003\">131157003</a></td><td>Blood group A variant</td></tr><tr><td><a href=\"http://snomed.info/id/131156007\">131156007</a></td><td>Blood group A>el<</td></tr><tr><td><a href=\"http://snomed.info/id/131155006\">131155006</a></td><td>Blood group A>end<</td></tr><tr><td><a href=\"http://snomed.info/id/131154005\">131154005</a></td><td>Blood group A>y<</td></tr><tr><td><a href=\"http://snomed.info/id/131153004\">131153004</a></td><td>Blood group A>m<</td></tr><tr><td><a href=\"http://snomed.info/id/131152009\">131152009</a></td><td>Blood group A>x<</td></tr><tr><td><a href=\"http://snomed.info/id/131151002\">131151002</a></td><td>Blood group A>3<</td></tr><tr><td><a href=\"http://snomed.info/id/131150001\">131150001</a></td><td>Blood group A>2<</td></tr><tr><td><a href=\"http://snomed.info/id/131149001\">131149001</a></td><td>Blood group A>1<</td></tr><tr><td><a href=\"http://snomed.info/id/115940004\">115940004</a></td><td>Blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115867006\">115867006</a></td><td>Ch-Rg- phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115866002\">115866002</a></td><td>Chido-Rodgers blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115861007\">115861007</a></td><td>Inab phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115860008\">115860008</a></td><td>Cromer blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115855009\">115855009</a></td><td>Gerbich negative phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115854008\">115854008</a></td><td>Gerbich positive phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115853002\">115853002</a></td><td>Gerbich blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115852007\">115852007</a></td><td>Co(a-b-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115851000\">115851000</a></td><td>Colton blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115845005\">115845005</a></td><td>McLeod phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115844009\">115844009</a></td><td>Kx blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115839002\">115839002</a></td><td>Kell>mod< phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115838005\">115838005</a></td><td>Kell>null< phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115837000\">115837000</a></td><td>Kell blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115835008\">115835008</a></td><td>Fy(a-b-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115834007\">115834007</a></td><td>Duffy blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115833001\">115833001</a></td><td>In(Jk) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115832006\">115832006</a></td><td>JkJk phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115831004\">115831004</a></td><td>Jk(a-b-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115830003\">115830003</a></td><td>Kidd blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115827005\">115827005</a></td><td>Lutheran weak phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115826001\">115826001</a></td><td>Acquired Lutheran negative phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115825002\">115825002</a></td><td>XS2 phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115824003\">115824003</a></td><td>In(Lu) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115823009\">115823009</a></td><td>LuLu phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115822004\">115822004</a></td><td>Lutheran negative phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115821006\">115821006</a></td><td>Lutheran blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115805001\">115805001</a></td><td>En(a-)(UK) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115804002\">115804002</a></td><td>En(a-)(Fin) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115803008\">115803008</a></td><td>En(a-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115802003\">115802003</a></td><td>U- phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115801005\">115801005</a></td><td>M^k^M^k^ phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115800006\">115800006</a></td><td>MNS blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115799007\">115799007</a></td><td>LW(a-b-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115798004\">115798004</a></td><td>Landsteiner-Wiener phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115797009\">115797009</a></td><td>P>2<^k^ phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115796000\">115796000</a></td><td>P>1<^k^ phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115795001\">115795001</a></td><td>P>1< phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115794002\">115794002</a></td><td>P blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115764008\">115764008</a></td><td>Inherited weak D phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115763002\">115763002</a></td><td>Trans weak D phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115762007\">115762007</a></td><td>Rh>mod< blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115761000\">115761000</a></td><td>Rr^-^ blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115760004\">115760004</a></td><td>X^o^rX^o^r blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115759009\">115759009</a></td><td>Rh>null< phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115758001\">115758001</a></td><td>Rh (Rhesus) blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115756002\">115756002</a></td><td>I>int< phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115755003\">115755003</a></td><td>I phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115754004\">115754004</a></td><td>i>2< phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115753005\">115753005</a></td><td>i>1< phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115752000\">115752000</a></td><td>i>adult< phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115751007\">115751007</a></td><td>i>cord< phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115750008\">115750008</a></td><td>I blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115749008\">115749008</a></td><td>Le(a-b-) phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115748000\">115748000</a></td><td>Lewis blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/115737007\">115737007</a></td><td>Blood group B>h<</td></tr><tr><td><a href=\"http://snomed.info/id/115736003\">115736003</a></td><td>Blood group A>h<</td></tr><tr><td><a href=\"http://snomed.info/id/115735004\">115735004</a></td><td>Blood group Para-Bombay</td></tr><tr><td><a href=\"http://snomed.info/id/115734000\">115734000</a></td><td>Blood group O>h< Bombay Reunion type</td></tr><tr><td><a href=\"http://snomed.info/id/115732001\">115732001</a></td><td>Blood group O>h< Bombay Indian type</td></tr><tr><td><a href=\"http://snomed.info/id/115731008\">115731008</a></td><td>Blood group O>h< Bombay</td></tr><tr><td><a href=\"http://snomed.info/id/115730009\">115730009</a></td><td>Hh blood group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/112149005\">112149005</a></td><td>Blood group B</td></tr><tr><td><a href=\"http://snomed.info/id/112144000\">112144000</a></td><td>Blood group A</td></tr><tr><td><a href=\"http://snomed.info/id/112143006\">112143006</a></td><td>ABO group phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/103225004\">103225004</a></td><td>P>2< phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/89109006\">89109006</a></td><td>Weak D phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/88942003\">88942003</a></td><td>Blood group A>2<B</td></tr><tr><td><a href=\"http://snomed.info/id/81835007\">81835007</a></td><td>Weak c phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/79248008\">79248008</a></td><td>Blood group A>1<B</td></tr><tr><td><a href=\"http://snomed.info/id/74836001\">74836001</a></td><td>Secretor gene present (Se)</td></tr><tr><td><a href=\"http://snomed.info/id/65087006\">65087006</a></td><td>Weak M phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/64553001\">64553001</a></td><td>Secretor gene absent (se)</td></tr><tr><td><a href=\"http://snomed.info/id/58460004\">58460004</a></td><td>Blood group O</td></tr><tr><td><a href=\"http://snomed.info/id/57652005\">57652005</a></td><td>Weak V phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/45597001\">45597001</a></td><td>Blood group A>3<B</td></tr><tr><td><a href=\"http://snomed.info/id/38194003\">38194003</a></td><td>Weak e phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/34850003\">34850003</a></td><td>Weak Fy^b^ phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/25384006\">25384006</a></td><td>Weak S phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/25132006\">25132006</a></td><td>Weak N phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/24403008\">24403008</a></td><td>p phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/16345006\">16345006</a></td><td>Weak G phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/6800004\">6800004</a></td><td>Weak E phenotype</td></tr><tr><td><a href=\"http://snomed.info/id/3067005\">3067005</a></td><td>Weak C phenotype</td></tr></table></li></ul></div>"^^rdf:XMLLiteral ] ; # fhir:extension ( [ fhir:url [ fhir:v "http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm"^^xsd:anyURI ] ; fhir:value [ a fhir:integer ; fhir:v 1 ] ] [ fhir:url [ fhir:v "http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status"^^xsd:anyURI ] ; fhir:value [ a fhir:code ; fhir:v "draft" ] ] ) ; # fhir:url [ fhir:v "http://terminology.ehdsi.eu/ValueSet/eHDSIBloodGroup"^^xsd:anyURI] ; # fhir:identifier ( [ fhir:system [ fhir:v "urn:ietf:rfc:3986"^^xsd:anyURI ] ; fhir:value [ fhir:v "urn:oid:1.3.6.1.4.1.12559.11.10.1.3.1.42.20" ] ] ) ; # fhir:version [ fhir:v "0.1.1"] ; # fhir:name [ fhir:v "EHDSIBloodGroupLab"] ; # fhir:title [ fhir:v "eHDSI Blood Group for laboratory result value"] ; # fhir:status [ fhir:v "active"] ; # fhir:experimental [ fhir:v false] ; # fhir:date [ fhir:v "2025-05-16T14:33:24+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 encode the value of a patient's laboratory blood group result"] ; # fhir:jurisdiction ( [ ( fhir:coding [ fhir:system [ fhir:v "http://unstats.un.org/unsd/methods/m49/m49.htm"^^xsd:anyURI ] ; fhir:code [ fhir:v "150" ] ; fhir:display [ fhir:v "Europe" ] ] ) ] ) ; # 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:concept [ fhir:code [ fhir:v "1162255003" ] ; fhir:display [ fhir:v "Fetal blood group Rhesus positive" ] ] [ fhir:code [ fhir:v "1162254004" ] ; fhir:display [ fhir:v "Fetal blood group Rhesus negative" ] ] [ fhir:code [ fhir:v "733120009" ] ; fhir:display [ fhir:v "Rhc positive" ] ] [ fhir:code [ fhir:v "733119003" ] ; fhir:display [ fhir:v "Rhc negative" ] ] [ fhir:code [ fhir:v "406009006" ] ; fhir:display [ fhir:v "CDE haplotype" ] ] [ fhir:code [ fhir:v "406008003" ] ; fhir:display [ fhir:v "CdE haplotype" ] ] [ fhir:code [ fhir:v "406007008" ] ; fhir:display [ fhir:v "cDe haplotype" ] ] [ fhir:code [ fhir:v "406006004" ] ; fhir:display [ fhir:v "cDE haplotype" ] ] [ fhir:code [ fhir:v "406005000" ] ; fhir:display [ fhir:v "CDe haplotype" ] ] [ fhir:code [ fhir:v "406004001" ] ; fhir:display [ fhir:v "cdE haplotype" ] ] [ fhir:code [ fhir:v "406003007" ] ; fhir:display [ fhir:v "Cde haplotype" ] ] [ fhir:code [ fhir:v "406002002" ] ; fhir:display [ fhir:v "cde haplotype" ] ] [ fhir:code [ fhir:v "405901003" ] ; fhir:display [ fhir:v "P1- phenotype" ] ] [ fhir:code [ fhir:v "405900002" ] ; fhir:display [ fhir:v "P1+ phenotype" ] ] [ fhir:code [ fhir:v "405899007" ] ; fhir:display [ fhir:v "K-k+ phenotype" ] ] [ fhir:code [ fhir:v "405898004" ] ; fhir:display [ fhir:v "K-k- phenotype" ] ] [ fhir:code [ fhir:v "405897009" ] ; fhir:display [ fhir:v "K+k- phenotype" ] ] [ fhir:code [ fhir:v "405896000" ] ; fhir:display [ fhir:v "K+k+ phenotype" ] ] [ fhir:code [ fhir:v "405895001" ] ; fhir:display [ fhir:v "k+ phenotype" ] ] [ fhir:code [ fhir:v "405894002" ] ; fhir:display [ fhir:v "k- phenotype" ] ] [ fhir:code [ fhir:v "405893008" ] ; fhir:display [ fhir:v "K- phenotype" ] ] [ fhir:code [ fhir:v "405892003" ] ; fhir:display [ fhir:v "K+ phenotype" ] ] [ fhir:code [ fhir:v "405891005" ] ; fhir:display [ fhir:v "S+s- phenotype" ] ] [ fhir:code [ fhir:v "405890006" ] ; fhir:display [ fhir:v "S-s- phenotype" ] ] [ fhir:code [ fhir:v "405889002" ] ; fhir:display [ fhir:v "S-s+ phenotype" ] ] [ fhir:code [ fhir:v "405888005" ] ; fhir:display [ fhir:v "S+s+ phenotype" ] ] [ fhir:code [ fhir:v "405887000" ] ; fhir:display [ fhir:v "s+ phenotype" ] ] [ fhir:code [ fhir:v "405886009" ] ; fhir:display [ fhir:v "s- phenotype" ] ] [ fhir:code [ fhir:v "405885008" ] ; fhir:display [ fhir:v "S+ phenotype" ] ] [ fhir:code [ fhir:v "405884007" ] ; fhir:display [ fhir:v "S- phenotype" ] ] [ fhir:code [ fhir:v "405883001" ] ; fhir:display [ fhir:v "M-N+ phenotype" ] ] [ fhir:code [ fhir:v "405882006" ] ; fhir:display [ fhir:v "M+N+ phenotype" ] ] [ fhir:code [ fhir:v "405881004" ] ; fhir:display [ fhir:v "M+N- phenotype" ] ] [ fhir:code [ fhir:v "405880003" ] ; fhir:display [ fhir:v "M-N- phenotype" ] ] [ fhir:code [ fhir:v "405879001" ] ; fhir:display [ fhir:v "N- phenotype" ] ] [ fhir:code [ fhir:v "405878009" ] ; fhir:display [ fhir:v "N+ phenotype" ] ] [ fhir:code [ fhir:v "405877004" ] ; fhir:display [ fhir:v "Le(a+b+) phenotype" ] ] [ fhir:code [ fhir:v "405876008" ] ; fhir:display [ fhir:v "M- phenotype" ] ] [ fhir:code [ fhir:v "405875007" ] ; fhir:display [ fhir:v "M+ phenotype" ] ] [ fhir:code [ fhir:v "405874006" ] ; fhir:display [ fhir:v "Lu(b-) phenotype" ] ] [ fhir:code [ fhir:v "405873000" ] ; fhir:display [ fhir:v "Lu(b+) phenotype" ] ] [ fhir:code [ fhir:v "405872005" ] ; fhir:display [ fhir:v "Lu(a+) phenotype" ] ] [ fhir:code [ fhir:v "405871003" ] ; fhir:display [ fhir:v "Lu(a-) phenotype" ] ] [ fhir:code [ fhir:v "405870002" ] ; 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 "405868006" ] ; fhir:display [ fhir:v "Lu(a-b+) phenotype" ] ] [ fhir:code [ fhir:v "405866005" ] ; fhir:display [ fhir:v "Le(b-) phenotype" ] ] [ fhir:code [ fhir:v "405865009" ] ; fhir:display [ fhir:v "Le(b+) phenotype" ] ] [ fhir:code [ fhir:v "405864008" ] ; fhir:display [ fhir:v "Le(a+) phenotype" ] ] [ fhir:code [ fhir:v "405863002" ] ; fhir:display [ fhir:v "Le(a-) phenotype" ] ] [ fhir:code [ fhir:v "405862007" ] ; fhir:display [ fhir:v "Le(a-b+) phenotype" ] ] [ fhir:code [ fhir:v "405861000" ] ; fhir:display [ fhir:v "Le(a+b-) phenotype" ] ] [ fhir:code [ fhir:v "405860004" ] ; fhir:display [ fhir:v "Jk(b-) phenotype" ] ] [ fhir:code [ fhir:v "405859009" ] ; fhir:display [ fhir:v "Jk(b+) phenotype" ] ] [ fhir:code [ fhir:v "405858001" ] ; fhir:display [ fhir:v "Jk(a-b+) phenotype" ] ] [ fhir:code [ fhir:v "405857006" ] ; fhir:display [ fhir:v "Jk(a-) phenotype" ] ] [ fhir:code [ fhir:v "405856002" ] ; fhir:display [ fhir:v "Jk(a+b-) phenotype" ] ] [ fhir:code [ fhir:v "405855003" ] ; fhir:display [ fhir:v "Jk(a+b+) phenotype" ] ] [ fhir:code [ fhir:v "405854004" ] ; fhir:display [ fhir:v "Jk(a+) phenotype" ] ] [ fhir:code [ fhir:v "405853005" ] ; fhir:display [ fhir:v "Fy(b+) phenotype" ] ] [ fhir:code [ fhir:v "405852000" ] ; fhir:display [ fhir:v "Fy(b-) phenotype" ] ] [ fhir:code [ fhir:v "405851007" ] ; fhir:display [ fhir:v "Fy(a+) phenotype" ] ] [ fhir:code [ fhir:v "405850008" ] ; fhir:display [ fhir:v "Fy(a-) phenotype" ] ] [ fhir:code [ fhir:v "405849008" ] ; 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 "405847005" ] ; fhir:display [ fhir:v "Fy(a+b-) phenotype" ] ] [ fhir:code [ fhir:v "365645007" ] ; fhir:display [ fhir:v "Finding of Rh (Rhesus) genotype" ] ] [ fhir:code [ fhir:v "365643000" ] ; fhir:display [ fhir:v "Rh antigen type - finding" ] ] [ fhir:code [ fhir:v "365642005" ] ; fhir:display [ fhir:v "Blood group antigen type - finding" ] ] [ fhir:code [ fhir:v "365641003" ] ; fhir:display [ fhir:v "Minor blood groups - finding" ] ] [ fhir:code [ fhir:v "365640002" ] ; fhir:display [ fhir:v "Common composite blood groups - finding" ] ] [ fhir:code [ fhir:v "365638007" ] ; fhir:display [ fhir:v "Finding of Rh (Rhesus) blood group" ] ] [ fhir:code [ fhir:v "365637002" ] ; fhir:display [ fhir:v "ABO blood group - finding" ] ] [ fhir:code [ fhir:v "278154007" ] ; fhir:display [ fhir:v "Blood group AB Rh(D) negative" ] ] [ fhir:code [ fhir:v "278153001" ] ; fhir:display [ fhir:v "Blood group B Rh(D) negative" ] ] [ fhir:code [ fhir:v "278152006" ] ; fhir:display [ fhir:v "Blood group A Rh(D) negative" ] ] [ fhir:code [ fhir:v "278151004" ] ; fhir:display [ fhir:v "Blood group AB Rh(D) positive" ] ] [ fhir:code [ fhir:v "278150003" ] ; fhir:display [ fhir:v "Blood group B Rh(D) positive" ] ] [ fhir:code [ fhir:v "278149003" ] ; fhir:display [ fhir:v "Blood group A Rh(D) positive" ] ] [ fhir:code [ fhir:v "278148006" ] ; fhir:display [ fhir:v "Blood group O Rh(D) negative" ] ] [ fhir:code [ fhir:v "278147001" ] ; fhir:display [ fhir:v "Blood group O Rh(D) positive" ] ] [ fhir:code [ fhir:v "250400003" ] ; fhir:display [ fhir:v "Low incidence antigen type" ] ] [ fhir:code [ fhir:v "250399005" ] ; fhir:display [ fhir:v "Kx antigen type" ] ] [ fhir:code [ fhir:v "250398002" ] ; fhir:display [ fhir:v "H antigen type" ] ] [ fhir:code [ fhir:v "250397007" ] ; fhir:display [ fhir:v "Chido-Rogers antigen type" ] ] [ fhir:code [ fhir:v "250396003" ] ; fhir:display [ fhir:v "Diego antigen type" ] ] [ fhir:code [ fhir:v "250395004" ] ; fhir:display [ fhir:v "Cartwright antigen type" ] ] [ fhir:code [ fhir:v "250394000" ] ; fhir:display [ fhir:v "Landsteiner-Weiner antigen type" ] ] [ fhir:code [ fhir:v "250392001" ] ; fhir:display [ fhir:v "MNS antigen type" ] ] [ fhir:code [ fhir:v "250391008" ] ; fhir:display [ fhir:v "Kidd antigen type" ] ] [ fhir:code [ fhir:v "250390009" ] ; fhir:display [ fhir:v "Duffy antigen type" ] ] [ fhir:code [ fhir:v "250389000" ] ; fhir:display [ fhir:v "Kell antigen type" ] ] [ fhir:code [ fhir:v "250376006" ] ; fhir:display [ fhir:v "Rh negative Du positive" ] ] [ fhir:code [ fhir:v "165751009" ] ; fhir:display [ fhir:v "Duffy blood group" ] ] [ fhir:code [ fhir:v "165747007" ] ; fhir:display [ fhir:v "RhD positive" ] ] [ fhir:code [ fhir:v "165746003" ] ; fhir:display [ fhir:v "RhD negative" ] ] [ fhir:code [ fhir:v "165743006" ] ; fhir:display [ fhir:v "Blood group AB" ] ] [ fhir:code [ fhir:v "131181005" ] ; fhir:display [ fhir:v "Leach type" ] ] [ fhir:code [ fhir:v "131180006" ] ; fhir:display [ fhir:v "Melasian type" ] ] [ fhir:code [ fhir:v "131179008" ] ; fhir:display [ fhir:v "Yus type" ] ] [ fhir:code [ fhir:v "131178000" ] ; fhir:display [ fhir:v "Gerbich type" ] ] [ fhir:code [ fhir:v "131169006" ] ; fhir:display [ fhir:v "Blood group O>Hm<^B^" ] ] [ fhir:code [ fhir:v "131168003" ] ; fhir:display [ fhir:v "Blood group O>Hm<^A^" ] ] [ fhir:code [ fhir:v "131167008" ] ; fhir:display [ fhir:v "Blood group O>Hm<" ] ] [ fhir:code [ fhir:v "131166004" ] ; fhir:display [ fhir:v "Blood group O>m<^h^" ] ] [ fhir:code [ fhir:v "131165000" ] ; fhir:display [ fhir:v "Blood group B>m<^h^" ] ] [ fhir:code [ fhir:v "131164001" ] ; fhir:display [ fhir:v "Blood group A>m<^h^" ] ] [ fhir:code [ fhir:v "131163007" ] ; fhir:display [ fhir:v "Blood group B>x<" ] ] [ fhir:code [ fhir:v "131162002" ] ; fhir:display [ fhir:v "Blood group B>w<" ] ] [ fhir:code [ fhir:v "131161009" ] ; fhir:display [ fhir:v "Blood group B>el<" ] ] [ fhir:code [ fhir:v "131160005" ] ; fhir:display [ fhir:v "Blood group B>m<" ] ] [ fhir:code [ fhir:v "131159000" ] ; fhir:display [ fhir:v "Blood group B>3<" ] ] [ fhir:code [ fhir:v "131158008" ] ; fhir:display [ fhir:v "Blood group B variant" ] ] [ fhir:code [ fhir:v "131157003" ] ; fhir:display [ fhir:v "Blood group A variant" ] ] [ fhir:code [ fhir:v "131156007" ] ; fhir:display [ fhir:v "Blood group A>el<" ] ] [ fhir:code [ fhir:v "131155006" ] ; fhir:display [ fhir:v "Blood group A>end<" ] ] [ fhir:code [ fhir:v "131154005" ] ; fhir:display [ fhir:v "Blood group A>y<" ] ] [ fhir:code [ fhir:v "131153004" ] ; fhir:display [ fhir:v "Blood group A>m<" ] ] [ fhir:code [ fhir:v "131152009" ] ; fhir:display [ fhir:v "Blood group A>x<" ] ] [ fhir:code [ fhir:v "131151002" ] ; fhir:display [ fhir:v "Blood group A>3<" ] ] [ fhir:code [ fhir:v "131150001" ] ; fhir:display [ fhir:v "Blood group A>2<" ] ] [ fhir:code [ fhir:v "131149001" ] ; fhir:display [ fhir:v "Blood group A>1<" ] ] [ fhir:code [ fhir:v "115940004" ] ; fhir:display [ fhir:v "Blood group phenotype" ] ] [ fhir:code [ fhir:v "115867006" ] ; fhir:display [ fhir:v "Ch-Rg- phenotype" ] ] [ fhir:code [ fhir:v "115866002" ] ; fhir:display [ fhir:v "Chido-Rodgers blood group phenotype" ] ] [ fhir:code [ fhir:v "115861007" ] ; fhir:display [ fhir:v "Inab phenotype" ] ] [ fhir:code [ fhir:v "115860008" ] ; fhir:display [ fhir:v "Cromer blood group phenotype" ] ] [ fhir:code [ fhir:v "115855009" ] ; fhir:display [ fhir:v "Gerbich negative phenotype" ] ] [ fhir:code [ fhir:v "115854008" ] ; fhir:display [ fhir:v "Gerbich positive phenotype" ] ] [ fhir:code [ fhir:v "115853002" ] ; fhir:display [ fhir:v "Gerbich blood group phenotype" ] ] [ fhir:code [ fhir:v "115852007" ] ; fhir:display [ fhir:v "Co(a-b-) phenotype" ] ] [ fhir:code [ fhir:v "115851000" ] ; fhir:display [ fhir:v "Colton blood group phenotype" ] ] [ fhir:code [ fhir:v "115845005" ] ; fhir:display [ fhir:v "McLeod phenotype" ] ] [ fhir:code [ fhir:v "115844009" ] ; fhir:display [ fhir:v "Kx blood group phenotype" ] ] [ fhir:code [ fhir:v "115839002" ] ; fhir:display [ fhir:v "Kell>mod< phenotype" ] ] [ fhir:code [ fhir:v "115838005" ] ; fhir:display [ fhir:v "Kell>null< phenotype" ] ] [ fhir:code [ fhir:v "115837000" ] ; fhir:display [ fhir:v "Kell blood group phenotype" ] ] [ fhir:code [ fhir:v "115835008" ] ; fhir:display [ fhir:v "Fy(a-b-) phenotype" ] ] [ fhir:code [ fhir:v "115834007" ] ; fhir:display [ fhir:v "Duffy blood group phenotype" ] ] [ fhir:code [ fhir:v "115833001" ] ; fhir:display [ fhir:v "In(Jk) phenotype" ] ] [ fhir:code [ fhir:v "115832006" ] ; fhir:display [ fhir:v "JkJk phenotype" ] ] [ fhir:code [ fhir:v "115831004" ] ; fhir:display [ fhir:v "Jk(a-b-) phenotype" ] ] [ fhir:code [ fhir:v "115830003" ] ; fhir:display [ fhir:v "Kidd blood group phenotype" ] ] [ fhir:code [ fhir:v "115827005" ] ; fhir:display [ fhir:v "Lutheran weak phenotype" ] ] [ fhir:code [ fhir:v "115826001" ] ; fhir:display [ fhir:v "Acquired Lutheran negative phenotype" ] ] [ fhir:code [ fhir:v "115825002" ] ; fhir:display [ fhir:v "XS2 phenotype" ] ] [ fhir:code [ fhir:v "115824003" ] ; fhir:display [ fhir:v "In(Lu) phenotype" ] ] [ fhir:code [ fhir:v "115823009" ] ; fhir:display [ fhir:v "LuLu phenotype" ] ] [ fhir:code [ fhir:v "115822004" ] ; fhir:display [ fhir:v "Lutheran negative phenotype" ] ] [ fhir:code [ fhir:v "115821006" ] ; fhir:display [ fhir:v "Lutheran blood group phenotype" ] ] [ fhir:code [ fhir:v "115805001" ] ; fhir:display [ fhir:v "En(a-)(UK) phenotype" ] ] [ fhir:code [ fhir:v "115804002" ] ; fhir:display [ fhir:v "En(a-)(Fin) phenotype" ] ] [ fhir:code [ fhir:v "115803008" ] ; fhir:display [ fhir:v "En(a-) phenotype" ] ] [ fhir:code [ fhir:v "115802003" ] ; fhir:display [ fhir:v "U- phenotype" ] ] [ fhir:code [ fhir:v "115801005" ] ; fhir:display [ fhir:v "M^k^M^k^ phenotype" ] ] [ fhir:code [ fhir:v "115800006" ] ; fhir:display [ fhir:v "MNS blood group phenotype" ] ] [ fhir:code [ fhir:v "115799007" ] ; fhir:display [ fhir:v "LW(a-b-) phenotype" ] ] [ fhir:code [ fhir:v "115798004" ] ; fhir:display [ fhir:v "Landsteiner-Wiener phenotype" ] ] [ fhir:code [ fhir:v "115797009" ] ; fhir:display [ fhir:v "P>2<^k^ phenotype" ] ] [ fhir:code [ fhir:v "115796000" ] ; fhir:display [ fhir:v "P>1<^k^ phenotype" ] ] [ fhir:code [ fhir:v "115795001" ] ; fhir:display [ fhir:v "P>1< phenotype" ] ] [ fhir:code [ fhir:v "115794002" ] ; fhir:display [ fhir:v "P blood group phenotype" ] ] [ fhir:code [ fhir:v "115764008" ] ; fhir:display [ fhir:v "Inherited weak D phenotype" ] ] [ fhir:code [ fhir:v "115763002" ] ; fhir:display [ fhir:v "Trans weak D phenotype" ] ] [ fhir:code [ fhir:v "115762007" ] ; fhir:display [ fhir:v "Rh>mod< blood group phenotype" ] ] [ fhir:code [ fhir:v "115761000" ] ; fhir:display [ fhir:v "Rr^-^ blood group phenotype" ] ] [ fhir:code [ fhir:v "115760004" ] ; fhir:display [ fhir:v "X^o^rX^o^r blood group phenotype" ] ] [ fhir:code [ fhir:v "115759009" ] ; fhir:display [ fhir:v "Rh>null< phenotype" ] ] [ fhir:code [ fhir:v "115758001" ] ; fhir:display [ fhir:v "Rh (Rhesus) blood group phenotype" ] ] [ fhir:code [ fhir:v "115756002" ] ; fhir:display [ fhir:v "I>int< phenotype" ] ] [ fhir:code [ fhir:v "115755003" ] ; fhir:display [ fhir:v "I phenotype" ] ] [ fhir:code [ fhir:v "115754004" ] ; fhir:display [ fhir:v "i>2< phenotype" ] ] [ fhir:code [ fhir:v "115753005" ] ; fhir:display [ fhir:v "i>1< phenotype" ] ] [ fhir:code [ fhir:v "115752000" ] ; fhir:display [ fhir:v "i>adult< phenotype" ] ] [ fhir:code [ fhir:v "115751007" ] ; fhir:display [ fhir:v "i>cord< phenotype" ] ] [ fhir:code [ fhir:v "115750008" ] ; fhir:display [ fhir:v "I blood group phenotype" ] ] [ fhir:code [ fhir:v "115749008" ] ; fhir:display [ fhir:v "Le(a-b-) phenotype" ] ] [ fhir:code [ fhir:v "115748000" ] ; fhir:display [ fhir:v "Lewis blood group phenotype" ] ] [ fhir:code [ fhir:v "115737007" ] ; fhir:display [ fhir:v "Blood group B>h<" ] ] [ fhir:code [ fhir:v "115736003" ] ; fhir:display [ fhir:v "Blood group A>h<" ] ] [ fhir:code [ fhir:v "115735004" ] ; fhir:display [ fhir:v "Blood group Para-Bombay" ] ] [ fhir:code [ fhir:v "115734000" ] ; fhir:display [ fhir:v "Blood group O>h< Bombay Reunion type" ] ] [ fhir:code [ fhir:v "115732001" ] ; fhir:display [ fhir:v "Blood group O>h< Bombay Indian type" ] ] [ fhir:code [ fhir:v "115731008" ] ; fhir:display [ fhir:v "Blood group O>h< Bombay" ] ] [ fhir:code [ fhir:v "115730009" ] ; fhir:display [ fhir:v "Hh blood group phenotype" ] ] [ fhir:code [ fhir:v "112149005" ] ; fhir:display [ fhir:v "Blood group B" ] ] [ fhir:code [ fhir:v "112144000" ] ; fhir:display [ fhir:v "Blood group A" ] ] [ fhir:code [ fhir:v "112143006" ] ; fhir:display [ fhir:v "ABO group phenotype" ] ] [ fhir:code [ fhir:v "103225004" ] ; fhir:display [ fhir:v "P>2< phenotype" ] ] [ fhir:code [ fhir:v "89109006" ] ; fhir:display [ fhir:v "Weak D phenotype" ] ] [ fhir:code [ fhir:v "88942003" ] ; fhir:display [ fhir:v "Blood group A>2<B" ] ] [ fhir:code [ fhir:v "81835007" ] ; fhir:display [ fhir:v "Weak c phenotype" ] ] [ fhir:code [ fhir:v "79248008" ] ; fhir:display [ fhir:v "Blood group A>1<B" ] ] [ fhir:code [ fhir:v "74836001" ] ; fhir:display [ fhir:v "Secretor gene present (Se)" ] ] [ fhir:code [ fhir:v "65087006" ] ; fhir:display [ fhir:v "Weak M phenotype" ] ] [ fhir:code [ fhir:v "64553001" ] ; fhir:display [ fhir:v "Secretor gene absent (se)" ] ] [ fhir:code [ fhir:v "58460004" ] ; fhir:display [ fhir:v "Blood group O" ] ] [ fhir:code [ fhir:v "57652005" ] ; fhir:display [ fhir:v "Weak V phenotype" ] ] [ fhir:code [ fhir:v "45597001" ] ; fhir:display [ fhir:v "Blood group A>3<B" ] ] [ fhir:code [ fhir:v "38194003" ] ; fhir:display [ fhir:v "Weak e phenotype" ] ] [ fhir:code [ fhir:v "34850003" ] ; fhir:display [ fhir:v "Weak Fy^b^ phenotype" ] ] [ fhir:code [ fhir:v "25384006" ] ; fhir:display [ fhir:v "Weak S phenotype" ] ] [ fhir:code [ fhir:v "25132006" ] ; fhir:display [ fhir:v "Weak N phenotype" ] ] [ fhir:code [ fhir:v "24403008" ] ; fhir:display [ fhir:v "p phenotype" ] ] [ fhir:code [ fhir:v "16345006" ] ; fhir:display [ fhir:v "Weak G phenotype" ] ] [ fhir:code [ fhir:v "6800004" ] ; fhir:display [ fhir:v "Weak E phenotype" ] ] [ fhir:code [ fhir:v "3067005" ] ; fhir:display [ fhir:v "Weak C phenotype" ] ] ) ] ) ] . #
IG © 2023+ MyHealth@Eu. Package myhealth.eu.fhir.laboratory#0.1.1 based on FHIR 4.0.1. Generated 2025-05-16
