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58275005: Variegate porphyria (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
498125013 Protoporphyrinogen oxidase deficiency en Synonym Active Case insensitive SNOMED CT core
498126014 VP - Variegate porphyria en Synonym Active Case sensitive SNOMED CT core
498127017 Porphyria variegata en Synonym Active Case insensitive SNOMED CT core
796989016 Variegate porphyria (disorder) en Fully specified name Active Case insensitive SNOMED CT core
96847016 Variegate porphyria en Synonym Active Case insensitive SNOMED CT core
96848014 South African porphyria en Synonym Active Case sensitive SNOMED CT core
96849018 South African genetic porphyria en Synonym Active Case sensitive SNOMED CT core
96850018 Protocoproporphyria en Synonym Active Case insensitive SNOMED CT core
96851019 Dean-Barnes syndrome en Synonym Active Case sensitive SNOMED CT core
96852014 Mixed porphyria en Synonym Active Case insensitive SNOMED CT core


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 Some
Variegate porphyria Occurrence Congenital false Inferred relationship Some
Variegate porphyria Finding site Liver structure true Inferred relationship Some 1

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

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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