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237984008: Neurogenic muscle weakness, ataxia and retinitis pigmentosa (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
356686010 Neurogenic muscle weakness, ataxia and retinitis pigmentosa en Synonym Active Entire term case insensitive SNOMED CT core module
356687018 NARP - Neurogenic muscle weakness, ataxia and retinitis pigmentosa en Synonym Active Entire term case sensitive SNOMED CT core module
626798015 Neurogenic muscle weakness, ataxia and retinitis pigmentosa (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
Neurogenic muscle weakness, ataxia and retinitis pigmentosa Is a Disorder of pyruvate metabolism and mitochondrial respiratory chain true Inferred relationship Existential restriction modifier
Neurogenic muscle weakness, ataxia and retinitis pigmentosa Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Neurogenic muscle weakness, ataxia and retinitis pigmentosa Finding site Body system structure false Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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