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111386004: Homozygous porphyria cutanea tarda (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
178624018 Homozygous porphyria cutanea tarda en Synonym Active Case insensitive SNOMED CT core
187767010 Hepatoerythropoietic porphyria en Synonym Active Case insensitive SNOMED CT core
630960010 Homozygous porphyria cutanea tarda (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Homozygous porphyria cutanea tarda Occurrence Congenital false Inferred relationship Some
Homozygous porphyria cutanea tarda Finding site Skin structure true Inferred relationship Some 2
Homozygous porphyria cutanea tarda Finding site Liver structure true Inferred relationship Some 1
Homozygous porphyria cutanea tarda Is a Porphyria cutanea tarda true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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