HL7 FHIR Implementation Guide Laboratory Report
0.2.0 - trial-use Italy flag

This page is part of the HL7 FHIR Implementation Guide Laboratory Report (v0.2.0: Release 1) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version. For a full list of available versions, see the Directory of published versions

ValueSet: Risultato osservazione codificato gruppo sanguigno

Official URL: http://hl7.it/fhir/lab-report/ValueSet/valueset-observation-value-bloodgroup Version: 0.2.0
Active as of 2024-03-08 Computable Name: VsObservationBloodGroup

Copyright/Legal: This value set includes content from SNOMED CT, which is copyright © 2002+ International Health Terminology Standards Development Organisation (IHTSDO), and distributed by agreement between IHTSDO and HL7. Implementer use of SNOMED CT is not covered by this agreement

Valueset contenente i codici SNOMED di gruppo sanguigno per la risorsa Observation - Lab Report per la descrizione del risultato della rilevazione.

References

Logical Definition (CLD)

 

Expansion

Expansion based on SNOMED CT International edition 01-feb 2024

This value set expansion contains 207 concepts.

CodeSystemDisplay
  3067005http://snomed.info/sctBlood group antigen C^u^
  6800004http://snomed.info/sctBlood group antigen E^u^
  16345006http://snomed.info/sctBlood group antigen G^u^
  24403008http://snomed.info/sctP-null phenotype
  25132006http://snomed.info/sctBlood group N>2<
  25384006http://snomed.info/sctBlood group S>2<
  34850003http://snomed.info/sctBlood group antigen Fy^x^
  38194003http://snomed.info/sctBlood group antigen e^i^
  45597001http://snomed.info/sctBlood group A>3<B
  57652005http://snomed.info/sctBlood group antigen V^u^
  58460004http://snomed.info/sctBlood group O
  64553001http://snomed.info/sctSecretor gene absent (se)
  65087006http://snomed.info/sctBlood group M>2<
  74836001http://snomed.info/sctSecretor gene present (Se)
  79248008http://snomed.info/sctBlood group A>1<B
  81835007http://snomed.info/sctBlood group antigen c^v^
  88942003http://snomed.info/sctBlood group A>2<B
  89109006http://snomed.info/sctBlood group antigen D^u^
  103225004http://snomed.info/sctBlood group P>2<
  112143006http://snomed.info/sctABO group phenotype
  112144000http://snomed.info/sctBlood group A
  112149005http://snomed.info/sctBlood group B
  115730009http://snomed.info/sctHh blood group phenotype
  115731008http://snomed.info/sctBlood group O>h< Bombay
  115732001http://snomed.info/sctBlood group O>h< Bombay Indian type
  115734000http://snomed.info/sctBlood group O>h< Bombay Reunion type
  115735004http://snomed.info/sctBlood group Para-Bombay
  115736003http://snomed.info/sctBlood group A>h<
  115737007http://snomed.info/sctBlood group B>h<
  115748000http://snomed.info/sctLewis blood group phenotype
  115749008http://snomed.info/sctLe(a-b-) phenotype
  115750008http://snomed.info/sctI blood group phenotype
  115751007http://snomed.info/scti>cord< phenotype
  115752000http://snomed.info/scti>adult< phenotype
  115753005http://snomed.info/scti>1< phenotype
  115754004http://snomed.info/scti>2< phenotype
  115755003http://snomed.info/sctI phenotype
  115756002http://snomed.info/sctI>int< phenotype
  115758001http://snomed.info/sctRhesus blood group phenotype
  115759009http://snomed.info/sctRh>null< phenotype
  115760004http://snomed.info/sctX^o^rX^o^r blood group phenotype
  115761000http://snomed.info/sctRr^-^ blood group phenotype
  115762007http://snomed.info/sctRh>mod< blood group phenotype
  115763002http://snomed.info/sctTrans weak D phenotype
  115764008http://snomed.info/sctInherited weak D phenotype
  115794002http://snomed.info/sctP blood group phenotype
  115795001http://snomed.info/sctP>1< phenotype
  115796000http://snomed.info/sctP>1<^k^ phenotype
  115797009http://snomed.info/sctP>2<^k^ phenotype
  115798004http://snomed.info/sctLandsteiner-Wiener phenotype
  115799007http://snomed.info/sctLW(a-b-) phenotype
  115800006http://snomed.info/sctMNS blood group phenotype
  115801005http://snomed.info/sctM^k^M^k^ phenotype
  115802003http://snomed.info/sctU- phenotype
  115803008http://snomed.info/sctEn(a-) phenotype
  115804002http://snomed.info/sctEn(a-)(Fin) phenotype
  115805001http://snomed.info/sctEn(a-)(UK) phenotype
  115821006http://snomed.info/sctLutheran blood group phenotype
  115822004http://snomed.info/sctLutheran negative phenotype
  115823009http://snomed.info/sctLuLu phenotype
  115824003http://snomed.info/sctIn(Lu) phenotype
  115825002http://snomed.info/sctXS2 phenotype
  115826001http://snomed.info/sctAcquired Lu(a-b-) phenotype
  115827005http://snomed.info/sctLutheran weak phenotype
  115830003http://snomed.info/sctKidd blood group phenotype
  115831004http://snomed.info/sctJk(a-b-) phenotype
  115832006http://snomed.info/sctJkJk phenotype
  115833001http://snomed.info/sctIn(Jk) phenotype
  115834007http://snomed.info/sctDuffy blood group phenotype
  115835008http://snomed.info/sctFy(a-b-) phenotype
  115837000http://snomed.info/sctKell blood group phenotype
  115838005http://snomed.info/sctKell>null< phenotype
  115839002http://snomed.info/sctKell>mod< phenotype
  115844009http://snomed.info/sctKx blood group phenotype
  115845005http://snomed.info/sctMcLeod phenotype
  115851000http://snomed.info/sctColton blood group phenotype
  115852007http://snomed.info/sctCo(a-b-) phenotype
  115853002http://snomed.info/sctGerbich blood group phenotype
  115854008http://snomed.info/sctGerbich positive phenotype
  115855009http://snomed.info/sctGerbich negative phenotype
  115860008http://snomed.info/sctCromer blood group phenotype
  115861007http://snomed.info/sctInab phenotype
  115866002http://snomed.info/sctChido-Rodgers blood group phenotype
  115867006http://snomed.info/sctCh-Rg- phenotype
  115940004http://snomed.info/sctBlood group phenotype
  131149001http://snomed.info/sctBlood group A>1<
  131150001http://snomed.info/sctBlood group A>2<
  131151002http://snomed.info/sctBlood group A>3<
  131152009http://snomed.info/sctBlood group A>x<
  131153004http://snomed.info/sctBlood group A>m<
  131154005http://snomed.info/sctBlood group A>y<
  131155006http://snomed.info/sctBlood group A>end<
  131156007http://snomed.info/sctBlood group A>el<
  131157003http://snomed.info/sctBlood group antigen A variant
  131158008http://snomed.info/sctB subgroup
  131159000http://snomed.info/sctBlood group B>3<
  131160005http://snomed.info/sctBlood group B>m<
  131161009http://snomed.info/sctBlood group B>el<
  131162002http://snomed.info/sctBlood group B>w<
  131163007http://snomed.info/sctBlood group B>x<
  131164001http://snomed.info/sctBlood group A>m<^h^
  131165000http://snomed.info/sctBlood group B>m<^h^
  131166004http://snomed.info/sctBlood group O>m<^h^
  131167008http://snomed.info/sctBlood group O>Hm<
  131168003http://snomed.info/sctBlood group O>Hm<^A^
  131169006http://snomed.info/sctBlood group O>Hm<^B^
  131178000http://snomed.info/sctGerbich type
  131179008http://snomed.info/sctYus type
  131180006http://snomed.info/sctMelasian type
  131181005http://snomed.info/sctLeach type
  165743006http://snomed.info/sctGroup AB
  165746003http://snomed.info/sctRh negative
  165747007http://snomed.info/sctRhesus positive
  165751009http://snomed.info/sctDuffy blood group
  250376006http://snomed.info/sctRh negative Du positive
  250389000http://snomed.info/sctKell antigen type
  250390009http://snomed.info/sctDuffy antigen type
  250391008http://snomed.info/sctKidd antigen type
  250392001http://snomed.info/sctMNS antigen type
  250394000http://snomed.info/sctLandsteiner-Weiner antigen type
  250395004http://snomed.info/sctCartwright antigen type
  250396003http://snomed.info/sctDiego antigen type
  250397007http://snomed.info/sctChido-Rogers antigen type
  250398002http://snomed.info/sctH antigen type
  250399005http://snomed.info/sctKx antigen type
  250400003http://snomed.info/sctLow incidence antigen type
  278147001http://snomed.info/sctBlood group O Rh(D) positive
  278148006http://snomed.info/sctGroup O neg
  278149003http://snomed.info/sctBlood group A Rh(D) positive
  278150003http://snomed.info/sctGroup B pos
  278151004http://snomed.info/sctBlood group AB Rh(D) positive
  278152006http://snomed.info/sctGroup A neg
  278153001http://snomed.info/sctBlood group B Rh(D) negative
  278154007http://snomed.info/sctGroup AB neg
  365637002http://snomed.info/sctABO blood group - finding
  365638007http://snomed.info/sctFinding of Rhesus blood group (finding)
  365640002http://snomed.info/sctCommon composite blood groups - finding
  365641003http://snomed.info/sctMinor blood groups
  365642005http://snomed.info/sctBlood group antigen type - finding
  365643000http://snomed.info/sctRh antigen type
  365645007http://snomed.info/sctFinding of Rhesus genotype (finding)
  405847005http://snomed.info/sctFy(a+b-) phenotype (finding)
  405848000http://snomed.info/sctFy(a-b+) phenotype (finding)
  405849008http://snomed.info/sctFy(a+b+) phenotype (finding)
  405850008http://snomed.info/sctFy(a-) phenotype (finding)
  405851007http://snomed.info/sctFy(a+) phenotype (finding)
  405852000http://snomed.info/sctFy(b-) phenotype (finding)
  405853005http://snomed.info/sctFy(b+) phenotype (finding)
  405854004http://snomed.info/sctJk(a+) phenotype (finding)
  405855003http://snomed.info/sctJk(a+b+) phenotype (finding)
  405856002http://snomed.info/sctJk(a+b-) phenotype (finding)
  405857006http://snomed.info/sctJk(a-) phenotype (finding)
  405858001http://snomed.info/sctJk(a-b+) phenotype (finding)
  405859009http://snomed.info/sctJk(b+) phenotype (finding)
  405860004http://snomed.info/sctJk(b-) phenotype (finding)
  405861000http://snomed.info/sctLe(a+b-) phenotype (finding)
  405862007http://snomed.info/sctLe(a-b+) phenotype (finding)
  405863002http://snomed.info/sctLe(a-) phenotype (finding)
  405864008http://snomed.info/sctLe(a+) phenotype (finding)
  405865009http://snomed.info/sctLe(b+) phenotype (finding)
  405866005http://snomed.info/sctLe(b-) phenotype (finding)
  405868006http://snomed.info/sctLu(a-b+) phenotype (finding)
  405869003http://snomed.info/sctLu(a+b+) phenotype (finding)
  405870002http://snomed.info/sctLu(a+b-) phenotype (finding)
  405871003http://snomed.info/sctLu(a-) phenotype (finding)
  405872005http://snomed.info/sctLu(a+) phenotype (finding)
  405873000http://snomed.info/sctLu(b+) phenotype (finding)
  405874006http://snomed.info/sctLu(b-) phenotype (finding)
  405875007http://snomed.info/sctM+ phenotype (finding)
  405876008http://snomed.info/sctM- phenotype (finding)
  405877004http://snomed.info/sctLe(a+b+) phenotype (finding)
  405878009http://snomed.info/sctN+ phenotype (finding)
  405879001http://snomed.info/sctN- phenotype (finding)
  405880003http://snomed.info/sctM-N- phenotype (finding)
  405881004http://snomed.info/sctM+N- phenotype (finding)
  405882006http://snomed.info/sctM+N+ phenotype (finding)
  405883001http://snomed.info/sctM-N+ phenotype (finding)
  405884007http://snomed.info/sctS- phenotype (finding)
  405885008http://snomed.info/sctS+ phenotype (finding)
  405886009http://snomed.info/scts- phenotype (finding)
  405887000http://snomed.info/scts+ phenotype (finding)
  405888005http://snomed.info/sctS+s+ phenotype (finding)
  405889002http://snomed.info/sctS-s+ phenotype (finding)
  405890006http://snomed.info/sctS-s- phenotype (finding)
  405891005http://snomed.info/sctS+s- phenotype (finding)
  405892003http://snomed.info/sctK+ phenotype (finding)
  405893008http://snomed.info/sctK- phenotype (finding)
  405894002http://snomed.info/sctk- phenotype (finding)
  405895001http://snomed.info/sctk+ phenotype (finding)
  405896000http://snomed.info/sctK+k+ phenotype (finding)
  405897009http://snomed.info/sctK+k- phenotype (finding)
  405898004http://snomed.info/sctK-k- phenotype (finding)
  405899007http://snomed.info/sctK-k+ phenotype (finding)
  405900002http://snomed.info/sctP1+ phenotype (finding)
  405901003http://snomed.info/sctP1- phenotype (finding)
  406002002http://snomed.info/sctcde haplotype (finding)
  406003007http://snomed.info/sctCde haplotype (finding)
  406004001http://snomed.info/sctcdE haplotype (finding)
  406005000http://snomed.info/sctCDe haplotype (finding)
  406006004http://snomed.info/sctcDE haplotype (finding)
  406007008http://snomed.info/sctcDe haplotype (finding)
  406008003http://snomed.info/sctCdE haplotype (finding)
  406009006http://snomed.info/sctCDE haplotype (finding)
  733119003http://snomed.info/sctRhc negative (finding)
  733120009http://snomed.info/sctRhc positive (finding)
  1162254004http://snomed.info/sctFetal blood group Rhesus negative
  1162255003http://snomed.info/sctFetal blood group Rhesus positive (finding)

Explanation of the columns that may appear on this page:

Level A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies
System The source of the definition of the code (when the value set draws in codes defined elsewhere)
Code The code (used as the code in the resource instance)
Display The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
Definition An explanation of the meaning of the concept
Comments Additional notes about how to use the code