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238054000: Homozygous acute intermittent porphyria (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
356834015 Homozygous acute intermittent porphyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626883010 Homozygous acute intermittent porphyria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
356834015 Homozygous acute intermittent porphyria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
356834015 Homozygous acute intermittent porphyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626883010 Homozygous acute intermittent porphyria (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
626883010 Homozygous acute intermittent porphyria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5021701000241115 porphyrie aigue intermittente homozygote fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5021701000241115 porphyrie aigue intermittente homozygote fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Homozygous acute intermittent porphyria Is a Acute intermittent porphyria true Inferred relationship Existential restriction modifier (core metadata concept)
Homozygous acute intermittent porphyria Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Homozygous acute intermittent porphyria Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Homozygous acute intermittent porphyria Course Intermittent false Inferred relationship Existential restriction modifier (core metadata concept)
Homozygous acute intermittent porphyria Clinical course Intermittent true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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