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61164006: Erythropoietic coproporphyria (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
101637018 Erythropoietic coproporphyria en Synonym Active Entire term case insensitive SNOMED CT core module
800196014 Erythropoietic coproporphyria (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Erythropoietic coproporphyria Is a Hereditary coproporphyria true Inferred relationship Existential restriction modifier
Erythropoietic coproporphyria Occurrence Congenital false Inferred relationship Existential restriction modifier
Erythropoietic coproporphyria Finding site Structure of skin region false Inferred relationship Existential restriction modifier
Erythropoietic coproporphyria Finding site Pulmonary valve structure false Inferred relationship Existential restriction modifier
Erythropoietic coproporphyria Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier
Erythropoietic coproporphyria Finding site Liver structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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