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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<status value="generated"/>
<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>
</text>
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<name value="EHDSIBloodGroupLab"/>
<title value="eHDSI Blood Group for laboratory result value"/>
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<date value="2025-06-06T10:40:10+00:00"/>
<publisher value="MyHealth@Eu"/>
<contact>
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<description
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<coding>
<system value="http://unstats.un.org/unsd/methods/m49/m49.htm"/>
<code value="150"/>
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<copyright
value="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."/>
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<display value="Cartwright antigen type"/>
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<code value="131180006"/>
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<display value="Kell blood group phenotype"/>
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<display value="Jk(a-b-) phenotype"/>
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<display value="Kidd blood group phenotype"/>
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<concept>
<code value="115827005"/>
<display value="Lutheran weak phenotype"/>
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<concept>
<code value="115826001"/>
<display value="Acquired Lutheran negative phenotype"/>
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<display value="Lutheran blood group phenotype"/>
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<display value="En(a-)(UK) phenotype"/>
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<concept>
<code value="115804002"/>
<display value="En(a-)(Fin) phenotype"/>
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<concept>
<code value="115803008"/>
<display value="En(a-) phenotype"/>
</concept>
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<code value="115802003"/>
<display value="U- phenotype"/>
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<code value="115801005"/>
<display value="M^k^M^k^ phenotype"/>
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<code value="115800006"/>
<display value="MNS blood group phenotype"/>
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<display value="LW(a-b-) phenotype"/>
</concept>
<concept>
<code value="115798004"/>
<display value="Landsteiner-Wiener phenotype"/>
</concept>
<concept>
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<display value="P>2<^k^ phenotype"/>
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<concept>
<code value="115796000"/>
<display value="P>1<^k^ phenotype"/>
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<display value="P>1< phenotype"/>
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<concept>
<code value="115794002"/>
<display value="P blood group phenotype"/>
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<concept>
<code value="115764008"/>
<display value="Inherited weak D phenotype"/>
</concept>
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<code value="115763002"/>
<display value="Trans weak D phenotype"/>
</concept>
<concept>
<code value="115762007"/>
<display value="Rh>mod< blood group phenotype"/>
</concept>
<concept>
<code value="115761000"/>
<display value="Rr^-^ blood group phenotype"/>
</concept>
<concept>
<code value="115760004"/>
<display value="X^o^rX^o^r blood group phenotype"/>
</concept>
<concept>
<code value="115759009"/>
<display value="Rh>null< phenotype"/>
</concept>
<concept>
<code value="115758001"/>
<display value="Rh (Rhesus) blood group phenotype"/>
</concept>
<concept>
<code value="115756002"/>
<display value="I>int< phenotype"/>
</concept>
<concept>
<code value="115755003"/>
<display value="I phenotype"/>
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<concept>
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<display value="i>2< phenotype"/>
</concept>
<concept>
<code value="115753005"/>
<display value="i>1< phenotype"/>
</concept>
<concept>
<code value="115752000"/>
<display value="i>adult< phenotype"/>
</concept>
<concept>
<code value="115751007"/>
<display value="i>cord< phenotype"/>
</concept>
<concept>
<code value="115750008"/>
<display value="I blood group phenotype"/>
</concept>
<concept>
<code value="115749008"/>
<display value="Le(a-b-) phenotype"/>
</concept>
<concept>
<code value="115748000"/>
<display value="Lewis blood group phenotype"/>
</concept>
<concept>
<code value="115737007"/>
<display value="Blood group B>h<"/>
</concept>
<concept>
<code value="115736003"/>
<display value="Blood group A>h<"/>
</concept>
<concept>
<code value="115735004"/>
<display value="Blood group Para-Bombay"/>
</concept>
<concept>
<code value="115734000"/>
<display value="Blood group O>h< Bombay Reunion type"/>
</concept>
<concept>
<code value="115732001"/>
<display value="Blood group O>h< Bombay Indian type"/>
</concept>
<concept>
<code value="115731008"/>
<display value="Blood group O>h< Bombay"/>
</concept>
<concept>
<code value="115730009"/>
<display value="Hh blood group phenotype"/>
</concept>
<concept>
<code value="112149005"/>
<display value="Blood group B"/>
</concept>
<concept>
<code value="112144000"/>
<display value="Blood group A"/>
</concept>
<concept>
<code value="112143006"/>
<display value="ABO group phenotype"/>
</concept>
<concept>
<code value="103225004"/>
<display value="P>2< phenotype"/>
</concept>
<concept>
<code value="89109006"/>
<display value="Weak D phenotype"/>
</concept>
<concept>
<code value="88942003"/>
<display value="Blood group A>2<B"/>
</concept>
<concept>
<code value="81835007"/>
<display value="Weak c phenotype"/>
</concept>
<concept>
<code value="79248008"/>
<display value="Blood group A>1<B"/>
</concept>
<concept>
<code value="74836001"/>
<display value="Secretor gene present (Se)"/>
</concept>
<concept>
<code value="65087006"/>
<display value="Weak M phenotype"/>
</concept>
<concept>
<code value="64553001"/>
<display value="Secretor gene absent (se)"/>
</concept>
<concept>
<code value="58460004"/>
<display value="Blood group O"/>
</concept>
<concept>
<code value="57652005"/>
<display value="Weak V phenotype"/>
</concept>
<concept>
<code value="45597001"/>
<display value="Blood group A>3<B"/>
</concept>
<concept>
<code value="38194003"/>
<display value="Weak e phenotype"/>
</concept>
<concept>
<code value="34850003"/>
<display value="Weak Fy^b^ phenotype"/>
</concept>
<concept>
<code value="25384006"/>
<display value="Weak S phenotype"/>
</concept>
<concept>
<code value="25132006"/>
<display value="Weak N phenotype"/>
</concept>
<concept>
<code value="24403008"/>
<display value="p phenotype"/>
</concept>
<concept>
<code value="16345006"/>
<display value="Weak G phenotype"/>
</concept>
<concept>
<code value="6800004"/>
<display value="Weak E phenotype"/>
</concept>
<concept>
<code value="3067005"/>
<display value="Weak C phenotype"/>
</concept>
</include>
</compose>
</ValueSet>
IG © 2023+ MyHealth@Eu. Package myhealth.eu.fhir.laboratory#0.1.1 based on FHIR 4.0.1. Generated 2025-06-06
