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
| Page standards status: Draft | Maturity Level: 1 |
{
"resourceType" : "ValueSet",
"id" : "eHDSIBloodGroupLab",
"text" : {
"status" : "generated",
"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>"
},
"extension" : [
{
"url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm",
"valueInteger" : 1
},
{
"url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status",
"valueCode" : "draft"
}
],
"url" : "http://terminology.ehdsi.eu/ValueSet/eHDSIBloodGroup",
"identifier" : [
{
"system" : "urn:ietf:rfc:3986",
"value" : "urn:oid:1.3.6.1.4.1.12559.11.10.1.3.1.42.20"
}
],
"version" : "0.1.1",
"name" : "EHDSIBloodGroupLab",
"title" : "eHDSI Blood Group for laboratory result value",
"status" : "active",
"experimental" : false,
"date" : "2025-05-16T14:33:24+00:00",
"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 encode the value of a patient's laboratory blood group result",
"jurisdiction" : [
{
"coding" : [
{
"system" : "http://unstats.un.org/unsd/methods/m49/m49.htm",
"code" : "150",
"display" : "Europe"
}
]
}
],
"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" : "1162255003",
"display" : "Fetal blood group Rhesus positive"
},
{
"code" : "1162254004",
"display" : "Fetal blood group Rhesus negative"
},
{
"code" : "733120009",
"display" : "Rhc positive"
},
{
"code" : "733119003",
"display" : "Rhc negative"
},
{
"code" : "406009006",
"display" : "CDE haplotype"
},
{
"code" : "406008003",
"display" : "CdE haplotype"
},
{
"code" : "406007008",
"display" : "cDe haplotype"
},
{
"code" : "406006004",
"display" : "cDE haplotype"
},
{
"code" : "406005000",
"display" : "CDe haplotype"
},
{
"code" : "406004001",
"display" : "cdE haplotype"
},
{
"code" : "406003007",
"display" : "Cde haplotype"
},
{
"code" : "406002002",
"display" : "cde haplotype"
},
{
"code" : "405901003",
"display" : "P1- phenotype"
},
{
"code" : "405900002",
"display" : "P1+ phenotype"
},
{
"code" : "405899007",
"display" : "K-k+ phenotype"
},
{
"code" : "405898004",
"display" : "K-k- phenotype"
},
{
"code" : "405897009",
"display" : "K+k- phenotype"
},
{
"code" : "405896000",
"display" : "K+k+ phenotype"
},
{
"code" : "405895001",
"display" : "k+ phenotype"
},
{
"code" : "405894002",
"display" : "k- phenotype"
},
{
"code" : "405893008",
"display" : "K- phenotype"
},
{
"code" : "405892003",
"display" : "K+ phenotype"
},
{
"code" : "405891005",
"display" : "S+s- phenotype"
},
{
"code" : "405890006",
"display" : "S-s- phenotype"
},
{
"code" : "405889002",
"display" : "S-s+ phenotype"
},
{
"code" : "405888005",
"display" : "S+s+ phenotype"
},
{
"code" : "405887000",
"display" : "s+ phenotype"
},
{
"code" : "405886009",
"display" : "s- phenotype"
},
{
"code" : "405885008",
"display" : "S+ phenotype"
},
{
"code" : "405884007",
"display" : "S- phenotype"
},
{
"code" : "405883001",
"display" : "M-N+ phenotype"
},
{
"code" : "405882006",
"display" : "M+N+ phenotype"
},
{
"code" : "405881004",
"display" : "M+N- phenotype"
},
{
"code" : "405880003",
"display" : "M-N- phenotype"
},
{
"code" : "405879001",
"display" : "N- phenotype"
},
{
"code" : "405878009",
"display" : "N+ phenotype"
},
{
"code" : "405877004",
"display" : "Le(a+b+) phenotype"
},
{
"code" : "405876008",
"display" : "M- phenotype"
},
{
"code" : "405875007",
"display" : "M+ phenotype"
},
{
"code" : "405874006",
"display" : "Lu(b-) phenotype"
},
{
"code" : "405873000",
"display" : "Lu(b+) phenotype"
},
{
"code" : "405872005",
"display" : "Lu(a+) phenotype"
},
{
"code" : "405871003",
"display" : "Lu(a-) phenotype"
},
{
"code" : "405870002",
"display" : "Lu(a+b-) phenotype"
},
{
"code" : "405869003",
"display" : "Lu(a+b+) phenotype"
},
{
"code" : "405868006",
"display" : "Lu(a-b+) phenotype"
},
{
"code" : "405866005",
"display" : "Le(b-) phenotype"
},
{
"code" : "405865009",
"display" : "Le(b+) phenotype"
},
{
"code" : "405864008",
"display" : "Le(a+) phenotype"
},
{
"code" : "405863002",
"display" : "Le(a-) phenotype"
},
{
"code" : "405862007",
"display" : "Le(a-b+) phenotype"
},
{
"code" : "405861000",
"display" : "Le(a+b-) phenotype"
},
{
"code" : "405860004",
"display" : "Jk(b-) phenotype"
},
{
"code" : "405859009",
"display" : "Jk(b+) phenotype"
},
{
"code" : "405858001",
"display" : "Jk(a-b+) phenotype"
},
{
"code" : "405857006",
"display" : "Jk(a-) phenotype"
},
{
"code" : "405856002",
"display" : "Jk(a+b-) phenotype"
},
{
"code" : "405855003",
"display" : "Jk(a+b+) phenotype"
},
{
"code" : "405854004",
"display" : "Jk(a+) phenotype"
},
{
"code" : "405853005",
"display" : "Fy(b+) phenotype"
},
{
"code" : "405852000",
"display" : "Fy(b-) phenotype"
},
{
"code" : "405851007",
"display" : "Fy(a+) phenotype"
},
{
"code" : "405850008",
"display" : "Fy(a-) phenotype"
},
{
"code" : "405849008",
"display" : "Fy(a+b+) phenotype"
},
{
"code" : "405848000",
"display" : "Fy(a-b+) phenotype"
},
{
"code" : "405847005",
"display" : "Fy(a+b-) phenotype"
},
{
"code" : "365645007",
"display" : "Finding of Rh (Rhesus) genotype"
},
{
"code" : "365643000",
"display" : "Rh antigen type - finding"
},
{
"code" : "365642005",
"display" : "Blood group antigen type - finding"
},
{
"code" : "365641003",
"display" : "Minor blood groups - finding"
},
{
"code" : "365640002",
"display" : "Common composite blood groups - finding"
},
{
"code" : "365638007",
"display" : "Finding of Rh (Rhesus) blood group"
},
{
"code" : "365637002",
"display" : "ABO blood group - finding"
},
{
"code" : "278154007",
"display" : "Blood group AB Rh(D) negative"
},
{
"code" : "278153001",
"display" : "Blood group B Rh(D) negative"
},
{
"code" : "278152006",
"display" : "Blood group A Rh(D) negative"
},
{
"code" : "278151004",
"display" : "Blood group AB Rh(D) positive"
},
{
"code" : "278150003",
"display" : "Blood group B Rh(D) positive"
},
{
"code" : "278149003",
"display" : "Blood group A Rh(D) positive"
},
{
"code" : "278148006",
"display" : "Blood group O Rh(D) negative"
},
{
"code" : "278147001",
"display" : "Blood group O Rh(D) positive"
},
{
"code" : "250400003",
"display" : "Low incidence antigen type"
},
{
"code" : "250399005",
"display" : "Kx antigen type"
},
{
"code" : "250398002",
"display" : "H antigen type"
},
{
"code" : "250397007",
"display" : "Chido-Rogers antigen type"
},
{
"code" : "250396003",
"display" : "Diego antigen type"
},
{
"code" : "250395004",
"display" : "Cartwright antigen type"
},
{
"code" : "250394000",
"display" : "Landsteiner-Weiner antigen type"
},
{
"code" : "250392001",
"display" : "MNS antigen type"
},
{
"code" : "250391008",
"display" : "Kidd antigen type"
},
{
"code" : "250390009",
"display" : "Duffy antigen type"
},
{
"code" : "250389000",
"display" : "Kell antigen type"
},
{
"code" : "250376006",
"display" : "Rh negative Du positive"
},
{
"code" : "165751009",
"display" : "Duffy blood group"
},
{
"code" : "165747007",
"display" : "RhD positive"
},
{
"code" : "165746003",
"display" : "RhD negative"
},
{
"code" : "165743006",
"display" : "Blood group AB"
},
{
"code" : "131181005",
"display" : "Leach type"
},
{
"code" : "131180006",
"display" : "Melasian type"
},
{
"code" : "131179008",
"display" : "Yus type"
},
{
"code" : "131178000",
"display" : "Gerbich type"
},
{
"code" : "131169006",
"display" : "Blood group O>Hm<^B^"
},
{
"code" : "131168003",
"display" : "Blood group O>Hm<^A^"
},
{
"code" : "131167008",
"display" : "Blood group O>Hm<"
},
{
"code" : "131166004",
"display" : "Blood group O>m<^h^"
},
{
"code" : "131165000",
"display" : "Blood group B>m<^h^"
},
{
"code" : "131164001",
"display" : "Blood group A>m<^h^"
},
{
"code" : "131163007",
"display" : "Blood group B>x<"
},
{
"code" : "131162002",
"display" : "Blood group B>w<"
},
{
"code" : "131161009",
"display" : "Blood group B>el<"
},
{
"code" : "131160005",
"display" : "Blood group B>m<"
},
{
"code" : "131159000",
"display" : "Blood group B>3<"
},
{
"code" : "131158008",
"display" : "Blood group B variant"
},
{
"code" : "131157003",
"display" : "Blood group A variant"
},
{
"code" : "131156007",
"display" : "Blood group A>el<"
},
{
"code" : "131155006",
"display" : "Blood group A>end<"
},
{
"code" : "131154005",
"display" : "Blood group A>y<"
},
{
"code" : "131153004",
"display" : "Blood group A>m<"
},
{
"code" : "131152009",
"display" : "Blood group A>x<"
},
{
"code" : "131151002",
"display" : "Blood group A>3<"
},
{
"code" : "131150001",
"display" : "Blood group A>2<"
},
{
"code" : "131149001",
"display" : "Blood group A>1<"
},
{
"code" : "115940004",
"display" : "Blood group phenotype"
},
{
"code" : "115867006",
"display" : "Ch-Rg- phenotype"
},
{
"code" : "115866002",
"display" : "Chido-Rodgers blood group phenotype"
},
{
"code" : "115861007",
"display" : "Inab phenotype"
},
{
"code" : "115860008",
"display" : "Cromer blood group phenotype"
},
{
"code" : "115855009",
"display" : "Gerbich negative phenotype"
},
{
"code" : "115854008",
"display" : "Gerbich positive phenotype"
},
{
"code" : "115853002",
"display" : "Gerbich blood group phenotype"
},
{
"code" : "115852007",
"display" : "Co(a-b-) phenotype"
},
{
"code" : "115851000",
"display" : "Colton blood group phenotype"
},
{
"code" : "115845005",
"display" : "McLeod phenotype"
},
{
"code" : "115844009",
"display" : "Kx blood group phenotype"
},
{
"code" : "115839002",
"display" : "Kell>mod< phenotype"
},
{
"code" : "115838005",
"display" : "Kell>null< phenotype"
},
{
"code" : "115837000",
"display" : "Kell blood group phenotype"
},
{
"code" : "115835008",
"display" : "Fy(a-b-) phenotype"
},
{
"code" : "115834007",
"display" : "Duffy blood group phenotype"
},
{
"code" : "115833001",
"display" : "In(Jk) phenotype"
},
{
"code" : "115832006",
"display" : "JkJk phenotype"
},
{
"code" : "115831004",
"display" : "Jk(a-b-) phenotype"
},
{
"code" : "115830003",
"display" : "Kidd blood group phenotype"
},
{
"code" : "115827005",
"display" : "Lutheran weak phenotype"
},
{
"code" : "115826001",
"display" : "Acquired Lutheran negative phenotype"
},
{
"code" : "115825002",
"display" : "XS2 phenotype"
},
{
"code" : "115824003",
"display" : "In(Lu) phenotype"
},
{
"code" : "115823009",
"display" : "LuLu phenotype"
},
{
"code" : "115822004",
"display" : "Lutheran negative phenotype"
},
{
"code" : "115821006",
"display" : "Lutheran blood group phenotype"
},
{
"code" : "115805001",
"display" : "En(a-)(UK) phenotype"
},
{
"code" : "115804002",
"display" : "En(a-)(Fin) phenotype"
},
{
"code" : "115803008",
"display" : "En(a-) phenotype"
},
{
"code" : "115802003",
"display" : "U- phenotype"
},
{
"code" : "115801005",
"display" : "M^k^M^k^ phenotype"
},
{
"code" : "115800006",
"display" : "MNS blood group phenotype"
},
{
"code" : "115799007",
"display" : "LW(a-b-) phenotype"
},
{
"code" : "115798004",
"display" : "Landsteiner-Wiener phenotype"
},
{
"code" : "115797009",
"display" : "P>2<^k^ phenotype"
},
{
"code" : "115796000",
"display" : "P>1<^k^ phenotype"
},
{
"code" : "115795001",
"display" : "P>1< phenotype"
},
{
"code" : "115794002",
"display" : "P blood group phenotype"
},
{
"code" : "115764008",
"display" : "Inherited weak D phenotype"
},
{
"code" : "115763002",
"display" : "Trans weak D phenotype"
},
{
"code" : "115762007",
"display" : "Rh>mod< blood group phenotype"
},
{
"code" : "115761000",
"display" : "Rr^-^ blood group phenotype"
},
{
"code" : "115760004",
"display" : "X^o^rX^o^r blood group phenotype"
},
{
"code" : "115759009",
"display" : "Rh>null< phenotype"
},
{
"code" : "115758001",
"display" : "Rh (Rhesus) blood group phenotype"
},
{
"code" : "115756002",
"display" : "I>int< phenotype"
},
{
"code" : "115755003",
"display" : "I phenotype"
},
{
"code" : "115754004",
"display" : "i>2< phenotype"
},
{
"code" : "115753005",
"display" : "i>1< phenotype"
},
{
"code" : "115752000",
"display" : "i>adult< phenotype"
},
{
"code" : "115751007",
"display" : "i>cord< phenotype"
},
{
"code" : "115750008",
"display" : "I blood group phenotype"
},
{
"code" : "115749008",
"display" : "Le(a-b-) phenotype"
},
{
"code" : "115748000",
"display" : "Lewis blood group phenotype"
},
{
"code" : "115737007",
"display" : "Blood group B>h<"
},
{
"code" : "115736003",
"display" : "Blood group A>h<"
},
{
"code" : "115735004",
"display" : "Blood group Para-Bombay"
},
{
"code" : "115734000",
"display" : "Blood group O>h< Bombay Reunion type"
},
{
"code" : "115732001",
"display" : "Blood group O>h< Bombay Indian type"
},
{
"code" : "115731008",
"display" : "Blood group O>h< Bombay"
},
{
"code" : "115730009",
"display" : "Hh blood group phenotype"
},
{
"code" : "112149005",
"display" : "Blood group B"
},
{
"code" : "112144000",
"display" : "Blood group A"
},
{
"code" : "112143006",
"display" : "ABO group phenotype"
},
{
"code" : "103225004",
"display" : "P>2< phenotype"
},
{
"code" : "89109006",
"display" : "Weak D phenotype"
},
{
"code" : "88942003",
"display" : "Blood group A>2<B"
},
{
"code" : "81835007",
"display" : "Weak c phenotype"
},
{
"code" : "79248008",
"display" : "Blood group A>1<B"
},
{
"code" : "74836001",
"display" : "Secretor gene present (Se)"
},
{
"code" : "65087006",
"display" : "Weak M phenotype"
},
{
"code" : "64553001",
"display" : "Secretor gene absent (se)"
},
{
"code" : "58460004",
"display" : "Blood group O"
},
{
"code" : "57652005",
"display" : "Weak V phenotype"
},
{
"code" : "45597001",
"display" : "Blood group A>3<B"
},
{
"code" : "38194003",
"display" : "Weak e phenotype"
},
{
"code" : "34850003",
"display" : "Weak Fy^b^ phenotype"
},
{
"code" : "25384006",
"display" : "Weak S phenotype"
},
{
"code" : "25132006",
"display" : "Weak N phenotype"
},
{
"code" : "24403008",
"display" : "p phenotype"
},
{
"code" : "16345006",
"display" : "Weak G phenotype"
},
{
"code" : "6800004",
"display" : "Weak E phenotype"
},
{
"code" : "3067005",
"display" : "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
