Value Set eHDSIBloodGroupLab 2025‑05‑06 15:52:48

This terminology is a snapshot as of 2025‑05‑19 12:35:31. Terminologies may evolve over time. If you need recent (dynamic) versions of this terminology, please retrieve it from the source. Id 1.3.6.1.4.1.12559.11.10.1.3.1.42.105 Effective Date 2025‑05‑06 15:52:48 Status Final Version Label 202505 Name eHDSIBloodGroupLab Display Name eHDSIBloodGroupLab Copyright This artefact includes content from SNOMED Clinical Terms® (SNOMED CT®) which is copyright of the International Health Terminology Standards Development Organisation (IHTSDO). Implementers of these artefacts must have the appropriate SNOMED CT Affiliate license - for more information contact http://www.snomed.org/snomed-ct/getsnomed-ct or info@snomed.org. Source Code System 2.16.840.1.113883.6.96 - SNOMED Clinical Terms - FHIR: http://snomed.info/sct - HL7 V2: SCT Level/ Type Code Display Name Code System 0‑L 1162255003 Fetal blood group Rhesus positive SNOMED Clinical Terms 0‑L 1162254004 Fetal blood group Rhesus negative SNOMED Clinical Terms 0‑L 733120009 Rhc positive SNOMED Clinical Terms 0‑L 733119003 Rhc negative SNOMED Clinical Terms 0‑L 406009006 CDE haplotype SNOMED Clinical Terms 0‑L 406008003 CdE haplotype SNOMED Clinical Terms 0‑L 406007008 cDe haplotype SNOMED Clinical Terms 0‑L 406006004 cDE haplotype SNOMED Clinical Terms 0‑L 406005000 CDe haplotype SNOMED Clinical Terms 0‑L 406004001 cdE haplotype SNOMED Clinical Terms 0‑L 406003007 Cde haplotype SNOMED Clinical Terms 0‑L 406002002 cde haplotype SNOMED Clinical Terms 0‑L 405901003 P1- phenotype SNOMED Clinical Terms 0‑L 405900002 P1+ phenotype SNOMED Clinical Terms 0‑L 405899007 K-k+ phenotype SNOMED Clinical Terms 0‑L 405898004 K-k- phenotype SNOMED Clinical Terms 0‑L 405897009 K+k- phenotype SNOMED Clinical Terms 0‑L 405896000 K+k+ phenotype SNOMED Clinical Terms 0‑L 405895001 k+ phenotype SNOMED Clinical Terms 0‑L 405894002 k- phenotype SNOMED Clinical Terms 0‑L 405893008 K- phenotype SNOMED Clinical Terms 0‑L 405892003 K+ phenotype SNOMED Clinical Terms 0‑L 405891005 S+s- phenotype SNOMED Clinical Terms 0‑L 405890006 S-s- phenotype SNOMED Clinical Terms 0‑L 405889002 S-s+ phenotype SNOMED Clinical Terms 0‑L 405888005 S+s+ phenotype SNOMED Clinical Terms 0‑L 405887000 s+ phenotype SNOMED Clinical Terms 0‑L 405886009 s- phenotype SNOMED Clinical Terms 0‑L 405885008 S+ phenotype SNOMED Clinical Terms 0‑L 405884007 S- phenotype SNOMED Clinical Terms 0‑L 405883001 M-N+ phenotype SNOMED Clinical Terms 0‑L 405882006 M+N+ phenotype SNOMED Clinical Terms 0‑L 405881004 M+N- phenotype SNOMED Clinical Terms 0‑L 405880003 M-N- phenotype SNOMED Clinical Terms 0‑L 405879001 N- phenotype SNOMED Clinical Terms 0‑L 405878009 N+ phenotype SNOMED Clinical Terms 0‑L 405877004 Le(a+b+) phenotype SNOMED Clinical Terms 0‑L 405876008 M- phenotype SNOMED Clinical Terms 0‑L 405875007 M+ phenotype SNOMED Clinical Terms 0‑L 405874006 Lu(b-) phenotype SNOMED Clinical Terms 0‑L 405873000 Lu(b+) phenotype SNOMED Clinical Terms 0‑L 405872005 Lu(a+) phenotype SNOMED Clinical Terms 0‑L 405871003 Lu(a-) phenotype SNOMED Clinical Terms 0‑L 405870002 Lu(a+b-) phenotype SNOMED Clinical Terms 0‑L 405869003 Lu(a+b+) phenotype SNOMED Clinical Terms 0‑L 405868006 Lu(a-b+) phenotype SNOMED Clinical Terms 0‑L 405866005 Le(b-) phenotype SNOMED Clinical Terms 0‑L 405865009 Le(b+) phenotype SNOMED Clinical Terms 0‑L 405864008 Le(a+) phenotype SNOMED Clinical Terms 0‑L 405863002 Le(a-) phenotype SNOMED Clinical Terms 0‑L 405862007 Le(a-b+) phenotype SNOMED Clinical Terms 0‑L 405861000 Le(a+b-) phenotype SNOMED Clinical Terms 0‑L 405860004 Jk(b-) phenotype SNOMED Clinical Terms 0‑L 405859009 Jk(b+) phenotype SNOMED Clinical Terms 0‑L 405858001 Jk(a-b+) phenotype SNOMED Clinical Terms 0‑L 405857006 Jk(a-) phenotype SNOMED Clinical Terms 0‑L 405856002 Jk(a+b-) phenotype SNOMED Clinical Terms 0‑L 405855003 Jk(a+b+) phenotype SNOMED Clinical Terms 0‑L 405854004 Jk(a+) phenotype SNOMED Clinical Terms 0‑L 405853005 Fy(b+) phenotype SNOMED Clinical Terms 0‑L 405852000 Fy(b-) phenotype SNOMED Clinical Terms 0‑L 405851007 Fy(a+) phenotype SNOMED Clinical Terms 0‑L 405850008 Fy(a-) phenotype SNOMED Clinical Terms 0‑L 405849008 Fy(a+b+) phenotype SNOMED Clinical Terms 0‑L 405848000 Fy(a-b+) phenotype SNOMED Clinical Terms 0‑L 405847005 Fy(a+b-) phenotype SNOMED Clinical Terms 0‑L 365645007 Finding of Rh (Rhesus) genotype SNOMED Clinical Terms 0‑L 365643000 Rh antigen type - finding SNOMED Clinical Terms 0‑L 365642005 Blood group antigen type - finding SNOMED Clinical Terms 0‑L 365641003 Minor blood groups - finding SNOMED Clinical Terms 0‑L 365640002 Common composite blood groups - finding SNOMED Clinical Terms 0‑L 365638007 Finding of Rh (Rhesus) blood group SNOMED Clinical Terms 0‑L 365637002 ABO blood group - finding SNOMED Clinical Terms 0‑L 278154007 Blood group AB Rh(D) negative SNOMED Clinical Terms 0‑L 278153001 Blood group B Rh(D) negative SNOMED Clinical Terms 0‑L 278152006 Blood group A Rh(D) negative SNOMED Clinical Terms 0‑L 278151004 Blood group AB Rh(D) positive SNOMED Clinical Terms 0‑L 278150003 Blood group B Rh(D) positive SNOMED Clinical Terms 0‑L 278149003 Blood group A Rh(D) positive SNOMED Clinical Terms 0‑L 278148006 Blood group O Rh(D) negative SNOMED Clinical Terms 0‑L 278147001 Blood group O Rh(D) positive SNOMED Clinical Terms 0‑L 250400003 Low incidence antigen type SNOMED Clinical Terms 0‑L 250399005 Kx antigen type SNOMED Clinical Terms 0‑L 250398002 H antigen type SNOMED Clinical Terms 0‑L 250397007 Chido-Rogers antigen type SNOMED Clinical Terms 0‑L 250396003 Diego antigen type SNOMED Clinical Terms 0‑L 250395004 Cartwright antigen type SNOMED Clinical Terms 0‑L 250394000 Landsteiner-Weiner antigen type SNOMED Clinical Terms 0‑L 250392001 MNS antigen type SNOMED Clinical Terms 0‑L 250391008 Kidd antigen type SNOMED Clinical Terms 0‑L 250390009 Duffy antigen type SNOMED Clinical Terms 0‑L 250389000 Kell antigen type SNOMED Clinical Terms 0‑L 250376006 Rh negative Du positive SNOMED Clinical Terms 0‑L 165751009 Duffy blood group SNOMED Clinical Terms 0‑L 165747007 RhD positive SNOMED Clinical Terms 0‑L 165746003 RhD negative SNOMED Clinical Terms 0‑L 165743006 Blood group AB SNOMED Clinical Terms 0‑L 131181005 Leach type SNOMED Clinical Terms 0‑L 131180006 Melasian type SNOMED Clinical Terms 0‑L 131179008 Yus type SNOMED Clinical Terms 0‑L 131178000 Gerbich type SNOMED Clinical Terms 0‑L 131169006 Blood group O>Hm<^B^ SNOMED Clinical Terms 0‑L 131168003 Blood group O>Hm<^A^ SNOMED Clinical Terms 0‑L 131167008 Blood group O>Hm< SNOMED Clinical Terms 0‑L 131166004 Blood group O>m<^h^ SNOMED Clinical Terms 0‑L 131165000 Blood group B>m<^h^ SNOMED Clinical Terms 0‑L 131164001 Blood group A>m<^h^ SNOMED Clinical Terms 0‑L 131163007 Blood group B>x< SNOMED Clinical Terms 0‑L 131162002 Blood group B>w< SNOMED Clinical Terms 0‑L 131161009 Blood group B>el< SNOMED Clinical Terms 0‑L 131160005 Blood group B>m< SNOMED Clinical Terms 0‑L 131159000 Blood group B>3< SNOMED Clinical Terms 0‑L 131158008 Blood group B variant SNOMED Clinical Terms 0‑L 131157003 Blood group A variant SNOMED Clinical Terms 0‑L 131156007 Blood group A>el< SNOMED Clinical Terms 0‑L 131155006 Blood group A>end< SNOMED Clinical Terms 0‑L 131154005 Blood group A>y< SNOMED Clinical Terms 0‑L 131153004 Blood group A>m< SNOMED Clinical Terms 0‑L 131152009 Blood group A>x< SNOMED Clinical Terms 0‑L 131151002 Blood group A>3< SNOMED Clinical Terms 0‑L 131150001 Blood group A>2< SNOMED Clinical Terms 0‑L 131149001 Blood group A>1< SNOMED Clinical Terms 0‑L 115940004 Blood group phenotype SNOMED Clinical Terms 0‑L 115867006 Ch-Rg- phenotype SNOMED Clinical Terms 0‑L 115866002 Chido-Rodgers blood group phenotype SNOMED Clinical Terms 0‑L 115861007 Inab phenotype SNOMED Clinical Terms 0‑L 115860008 Cromer blood group phenotype SNOMED Clinical Terms 0‑L 115855009 Gerbich negative phenotype SNOMED Clinical Terms 0‑L 115854008 Gerbich positive phenotype SNOMED Clinical Terms 0‑L 115853002 Gerbich blood group phenotype SNOMED Clinical Terms 0‑L 115852007 Co(a-b-) phenotype SNOMED Clinical Terms 0‑L 115851000 Colton blood group phenotype SNOMED Clinical Terms 0‑L 115845005 McLeod phenotype SNOMED Clinical Terms 0‑L 115844009 Kx blood group phenotype SNOMED Clinical Terms 0‑L 115839002 Kell>mod< phenotype SNOMED Clinical Terms 0‑L 115838005 Kell>null< phenotype SNOMED Clinical Terms 0‑L 115837000 Kell blood group phenotype SNOMED Clinical Terms 0‑L 115835008 Fy(a-b-) phenotype SNOMED Clinical Terms 0‑L 115834007 Duffy blood group phenotype SNOMED Clinical Terms 0‑L 115833001 In(Jk) phenotype SNOMED Clinical Terms 0‑L 115832006 JkJk phenotype SNOMED Clinical Terms 0‑L 115831004 Jk(a-b-) phenotype SNOMED Clinical Terms 0‑L 115830003 Kidd blood group phenotype SNOMED Clinical Terms 0‑L 115827005 Lutheran weak phenotype SNOMED Clinical Terms 0‑L 115826001 Acquired Lutheran negative phenotype SNOMED Clinical Terms 0‑L 115825002 XS2 phenotype SNOMED Clinical Terms 0‑L 115824003 In(Lu) phenotype SNOMED Clinical Terms 0‑L 115823009 LuLu phenotype SNOMED Clinical Terms 0‑L 115822004 Lutheran negative phenotype SNOMED Clinical Terms 0‑L 115821006 Lutheran blood group phenotype SNOMED Clinical Terms 0‑L 115805001 En(a-)(UK) phenotype SNOMED Clinical Terms 0‑L 115804002 En(a-)(Fin) phenotype SNOMED Clinical Terms 0‑L 115803008 En(a-) phenotype SNOMED Clinical Terms 0‑L 115802003 U- phenotype SNOMED Clinical Terms 0‑L 115801005 M^k^M^k^ phenotype SNOMED Clinical Terms 0‑L 115800006 MNS blood group phenotype SNOMED Clinical Terms 0‑L 115799007 LW(a-b-) phenotype SNOMED Clinical Terms 0‑L 115798004 Landsteiner-Wiener phenotype SNOMED Clinical Terms 0‑L 115797009 P>2<^k^ phenotype SNOMED Clinical Terms 0‑L 115796000 P>1<^k^ phenotype SNOMED Clinical Terms 0‑L 115795001 P>1< phenotype SNOMED Clinical Terms 0‑L 115794002 P blood group phenotype SNOMED Clinical Terms 0‑L 115764008 Inherited weak D phenotype SNOMED Clinical Terms 0‑L 115763002 Trans weak D phenotype SNOMED Clinical Terms 0‑L 115762007 Rh>mod< blood group phenotype SNOMED Clinical Terms 0‑L 115761000 Rr^-^ blood group phenotype SNOMED Clinical Terms 0‑L 115760004 X^o^rX^o^r blood group phenotype SNOMED Clinical Terms 0‑L 115759009 Rh>null< phenotype SNOMED Clinical Terms 0‑L 115758001 Rh (Rhesus) blood group phenotype SNOMED Clinical Terms 0‑L 115756002 I>int< phenotype SNOMED Clinical Terms 0‑L 115755003 I phenotype SNOMED Clinical Terms 0‑L 115754004 i>2< phenotype SNOMED Clinical Terms 0‑L 115753005 i>1< phenotype SNOMED Clinical Terms 0‑L 115752000 i>adult< phenotype SNOMED Clinical Terms 0‑L 115751007 i>cord< phenotype SNOMED Clinical Terms 0‑L 115750008 I blood group phenotype SNOMED Clinical Terms 0‑L 115749008 Le(a-b-) phenotype SNOMED Clinical Terms 0‑L 115748000 Lewis blood group phenotype SNOMED Clinical Terms 0‑L 115737007 Blood group B>h< SNOMED Clinical Terms 0‑L 115736003 Blood group A>h< SNOMED Clinical Terms 0‑L 115735004 Blood group Para-Bombay SNOMED Clinical Terms 0‑L 115734000 Blood group O>h< Bombay Reunion type SNOMED Clinical Terms 0‑L 115732001 Blood group O>h< Bombay Indian type SNOMED Clinical Terms 0‑L 115731008 Blood group O>h< Bombay SNOMED Clinical Terms 0‑L 115730009 Hh blood group phenotype SNOMED Clinical Terms 0‑L 112149005 Blood group B SNOMED Clinical Terms 0‑L 112144000 Blood group A SNOMED Clinical Terms 0‑L 112143006 ABO group phenotype SNOMED Clinical Terms 0‑L 103225004 P>2< phenotype SNOMED Clinical Terms 0‑L 89109006 Weak D phenotype SNOMED Clinical Terms 0‑L 88942003 Blood group A>2<B SNOMED Clinical Terms 0‑L 81835007 Weak c phenotype SNOMED Clinical Terms 0‑L 79248008 Blood group A>1<B SNOMED Clinical Terms 0‑L 74836001 Secretor gene present (Se) SNOMED Clinical Terms 0‑L 65087006 Weak M phenotype SNOMED Clinical Terms 0‑L 64553001 Secretor gene absent (se) SNOMED Clinical Terms 0‑L 58460004 Blood group O SNOMED Clinical Terms 0‑L 57652005 Weak V phenotype SNOMED Clinical Terms 0‑L 45597001 Blood group A>3<B SNOMED Clinical Terms 0‑L 38194003 Weak e phenotype SNOMED Clinical Terms 0‑L 34850003 Weak Fy^b^ phenotype SNOMED Clinical Terms 0‑L 25384006 Weak S phenotype SNOMED Clinical Terms 0‑L 25132006 Weak N phenotype SNOMED Clinical Terms 0‑L 24403008 p phenotype SNOMED Clinical Terms 0‑L 16345006 Weak G phenotype SNOMED Clinical Terms 0‑L 6800004 Weak E phenotype SNOMED Clinical Terms 0‑L 3067005 Weak C phenotype SNOMED Clinical Terms Legenda: Type L=leaf, S=specializable, A=abstract, D=deprecated. 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