Laboratory Base Class FHIR Profiles
0.1 - Draft United States of America flag

Laboratory Base Class FHIR Profiles, published by HL7 International - Clinical Information Modeling Initiative. This is not an authorized publication; it is the continuous build for version 0.1). This version is based on the current content of https://github.com/HL7/cimi-labs/ and changes regularly. See the Directory of published versions

ValueSet: Lab Result Code value set (Experimental)

Official URL: http://hl7.org/fhir/us/cimi-labs/ValueSet/lab-result-code-value-set Version: 0.1
Draft as of 2023-08-02 Computable Name: LabResutlCode_VSET

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

A set of LOINC codes that describe laboratory tests.

References

Logical Definition (CLD)

This value set includes codes based on the following rules:

 

Expansion

This value set contains 193 concepts

Expansion based on SNOMED CT United States edition 01-Mar 2023

CodeSystemDisplay
  46800005http://snomed.info/sctNormal urine color
  449031000124109http://snomed.info/sctStraw-colored urine (finding)
  449131000124105http://snomed.info/sctAmber-colored urine (finding)
  167239007http://snomed.info/sctUrine colour abnormal
  449051000124102http://snomed.info/sctRed-colored urine (finding)
  449061000124100http://snomed.info/sctPurple-colored urine (finding)
  449071000124107http://snomed.info/sctPink-colored urine (finding)
  449081000124105http://snomed.info/sctOrange-colored urine (finding)
  449091000124108http://snomed.info/sctGreen-colored urine (finding)
  449101000124102http://snomed.info/sctBrown-colored urine (finding)
  449111000124104http://snomed.info/sctBlue-colored urine (finding)
  115940004http://snomed.info/sctBlood group phenotype
  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
  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
  250376006http://snomed.info/sctRh negative Du positive
  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
  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)
  733119003http://snomed.info/sctRhc negative (finding)
  733120009http://snomed.info/sctRhc positive (finding)
  52101004http://snomed.info/sctPresent (qualifier value)
  10828004http://snomed.info/sctPositive (qualifier value)
  2667000http://snomed.info/sctAbsent (qualifier value)
  260385009http://snomed.info/sctNegative (qualifier value)

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