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58275005: Variegate porphyria (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
96847016 Variegate porphyria en Synonym Active Entire term case insensitive SNOMED CT core module
96848014 South African porphyria en Synonym Active Entire term case sensitive SNOMED CT core module
96849018 South African genetic porphyria en Synonym Active Entire term case sensitive SNOMED CT core module
96850018 Protocoproporphyria en Synonym Active Entire term case insensitive SNOMED CT core module
96851019 Dean-Barnes syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
96852014 Mixed porphyria en Synonym Active Entire term case insensitive SNOMED CT core module
498125013 Protoporphyrinogen oxidase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
498126014 VP - Variegate porphyria en Synonym Active Entire term case sensitive SNOMED CT core module
498127017 Porphyria variegata en Synonym Active Entire term case insensitive SNOMED CT core module
796989016 Variegate porphyria (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Variegate porphyria Is a Hepatic porphyria true Inferred relationship Existential restriction modifier
Variegate porphyria Occurrence Congenital false Inferred relationship Existential restriction modifier
Variegate porphyria Finding site Liver structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Homozygous variegate porphyria Is a True Variegate porphyria Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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