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7425008: Hereditary coproporphyria (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module Reference Sets
13238015 Hereditary coproporphyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
13239011 Berger-Goldberg syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
13240013 CPO deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
13241012 CPRO deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
13242017 Porphyria hepatica II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
502646019 HCP - Hereditary coproporphyria en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
502647011 Coproporphyrinogen oxidase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
502649014 CPO - Coproporphyrinogen oxidase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
814729016 Hereditary coproporphyria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
762381000052110 ärftlig koproporfyri sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept) Swedish [International Organization for Standardization 639-1 code sv] language reference set (foundation metadata concept): Preferred (foundation metadata concept)

2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary coproporphyria Is a Multisystem disorder W-X false Inferred relationship Some
Hereditary coproporphyria Is a Hereditary disorder of the integument false Inferred relationship Some
Hereditary coproporphyria Is a Congenital anomaly of trunk false Inferred relationship Some
Hereditary coproporphyria Is a Cardiovascular system hereditary disorder false Inferred relationship Some
Hereditary coproporphyria Is a Heart disease false Inferred relationship Some
Hereditary coproporphyria Is a Hereditary disorder of nervous system false Inferred relationship Some
Hereditary coproporphyria Is a Porphyria false Inferred relationship Some
Hereditary coproporphyria Is a Congenital anomaly of integument false Inferred relationship Some
Hereditary coproporphyria Is a Disorder of the central nervous system (disorder) false Inferred relationship Some
Hereditary coproporphyria Finding site Structure of central nervous system (body structure) false Inferred relationship Some
Hereditary coproporphyria Finding site Pulmonary valve structure false Inferred relationship Some
Hereditary coproporphyria Occurrence Congenital false Inferred relationship Some
Hereditary coproporphyria Finding site Structure of skin region false Inferred relationship Some
Hereditary coproporphyria Is a Disorder of skin (disorder) false Inferred relationship Some
Hereditary coproporphyria Is a Pulmonary valve disorder false Inferred relationship Some
Hereditary coproporphyria Is a multisystemsjukdom false Inferred relationship Some
Hereditary coproporphyria Is a Disorder of porphyrin metabolism false Inferred relationship Some
Hereditary coproporphyria Is a Site-specific disorder of skin false Inferred relationship Some
Hereditary coproporphyria Is a Disorder of soft tissue of thoracic cavity false Inferred relationship Some
Hereditary coproporphyria Is a Congenital heart disease false Inferred relationship Some
Hereditary coproporphyria Is a Coproporphyria true Inferred relationship Some
Hereditary coproporphyria Is a Hepatic porphyria true Inferred relationship Some
Hereditary coproporphyria Finding site Liver structure true Inferred relationship Some 1
Hereditary coproporphyria Is a Digestive system hereditary disorder (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Homozygous hereditary coproporphyria Is a True Hereditary coproporphyria Inferred relationship Some
Erythropoietic coproporphyria Is a True Hereditary coproporphyria Inferred relationship Some

Reference Sets

Medical conditions, alert information reference set (foundation metadata concept)

GB English

US English

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