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FHIR R4 value sets / code systems - Codesystem IDs

 
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References to External Code Systems (1)
References to External Code Systems
Id Name Display Name
2.16.840.1.113883.6.96 SNOMED_CT SNOMED CT (all versions)
Code Systems Used in this Project (60)
Code Systems Used in this Project
Id Name Display Name
1.0.3166.1.2.2 ISO 3166 Part 1 Country Codes, 2nd Edition, Alpha-2 ISO 3166 Part 1 Country Codes, 2nd Edition, Alpha-2
1.0.4217 ISO 4217 Currency Codes ISO 4217 Currency Codes
1.2.36.1.2001.1005.17 Australian Vaccine Code Australian Vaccine Code
1.3.6.1.4.1.19376.1.2.3 IHE.FormatCode.cs IHE.FormatCode.cs
2.16.840.1.113883.18.108 Identifier type Identifier type
2.16.840.1.113883.18.231 Treatment Treatment
2.16.840.1.113883.18.283 Provider Role Provider Role
2.16.840.1.113883.18.284 Name Assembly Order Name Assembly Order
2.16.840.1.113883.18.29 Diagnostic Service Section ID Diagnostic Service Section ID
2.16.840.1.113883.18.58 Contact Role Contact Role
2.16.840.1.113883.3.26.1.1 NCI Thesaurus NCI Thesaurus
2.16.840.1.113883.3.912 Catalogue Of Somatic Mutations In Cancer Catalogue Of Somatic Mutations In Cancer
2.16.840.1.113883.4.873 OID for URIs created subject to IETF rules OID for URIs created subject to IETF rules
2.16.840.1.113883.5.1001 Act Mood Act Mood
2.16.840.1.113883.5.1008 Null Flavor Null Flavor
2.16.840.1.113883.5.1020 ProbabilityDistributionType ProbabilityDistributionType
2.16.840.1.113883.5.1022 GTSAbbreviation GTSAbbreviation
2.16.840.1.113883.5.1052 Act Site Act Site
2.16.840.1.113883.5.1064 Participation Mode Participation Mode
2.16.840.1.113883.5.110 Role Class Role Class
2.16.840.1.113883.5.111 Role Code Role Code
2.16.840.1.113883.5.1119 Address Use Address Use
2.16.840.1.113883.5.112 Route Of Administration Route Of Administration
2.16.840.1.113883.5.1122 EntityNamePartQualifierR2 EntityNamePartQualifierR2
2.16.840.1.113883.5.1123 DataOperation DataOperation
2.16.840.1.113883.5.139 TimingEvent TimingEvent
2.16.840.1.113883.5.2 MaritalStatus MaritalStatus
2.16.840.1.113883.5.33 DocumentCompletion DocumentCompletion
2.16.840.1.113883.5.4 Act Code Act Code
2.16.840.1.113883.5.40 EncounterSpecialCourtesy EncounterSpecialCourtesy
2.16.840.1.113883.5.43 Entity Name Part Qualifier Entity Name Part Qualifier
2.16.840.1.113883.5.45 Entity Name Use Entity Name Use
2.16.840.1.113883.5.8 Act Reason Act Reason
2.16.840.1.113883.5.83 Observation Interpretation Observation Interpretation
2.16.840.1.113883.5.88 Participation Function Participation Function
2.16.840.1.113883.5.90 ParticipationType ParticipationType
2.16.840.1.113883.6.1 Logical Observation Identifier Names and Codes Logical Observation Identifier Names and Codes
2.16.840.1.113883.6.10 IETF MIME IETF MIME
2.16.840.1.113883.6.101 Health Care Provider Taxonomy Health Care Provider Taxonomy
2.16.840.1.113883.6.12 Current Procedure Terminology 4 (CPT-4) Current Procedure Terminology 4 (CPT-4)
2.16.840.1.113883.6.121 Tags for the Identification of Languages Tags for the Identification of Languages
2.16.840.1.113883.6.24 ISO 11073-10101 Health informatics Point-of-care medical device communication - Nomenclature ISO 11073-10101 Health informatics Point-of-care medical device communication - Nomenclature
2.16.840.1.113883.6.280 The Reference Sequence (RefSeq) is one of the NCBI projects, the RefSeq collection aims to provide a comprehensive, integrated, non-redundant, well-annotated set of sequences, including genomic DNA, t ... The Reference Sequence (RefSeq) is one of the NCBI projects, the RefSeq collection aims to provide a comprehensive, integrated, non-redundant, well-annotated set of sequences, including genomic DNA, t ...
2.16.840.1.113883.6.281 HUGO Gene Nomenclature HUGO Gene Nomenclature
2.16.840.1.113883.6.282 HGVS nomenclatures are the guidelines for mutation nomenclature made by the Human Genome Variation Society. HGVS nomenclature can be used with the HL7 coded data type (code data type that accepts ex ... HGVS nomenclatures are the guidelines for mutation nomenclature made by the Human Genome Variation Society. HGVS nomenclature can be used with the HL7 coded data type (code data type that accepts ex ...
2.16.840.1.113883.6.284 The Short Genetic Variations database The Short Genetic Variations database
2.16.840.1.113883.6.3 ICD10 ICD10
2.16.840.1.113883.6.324 Ensembl genomic reference sequence Ensembl genomic reference sequence
2.16.840.1.113883.6.341 Human leukocyte antigen nomenclature Human leukocyte antigen nomenclature
2.16.840.1.113883.6.59 CVX CVX
2.16.840.1.113883.6.8 Unified Code for Units of Measure Unified Code for Units of Measure
2.16.840.1.113883.6.88 RxNorm RxNorm
http://example.com
http://unstats.un.org/unsd/methods/m49/m49.htm
http://www.ncbi.nlm.nih.gov/clinvar
http://www.sequenceontology.org
https://precision.fda.gov/apps/
https://precision.fda.gov/files/
https://precision.fda.gov/jobs/
https://www.iana.org/time-zones