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237984008: Neurogenic muscle weakness, ataxia and retinitis pigmentosa (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
356686010 Neurogenic muscle weakness, ataxia and retinitis pigmentosa en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
356687018 NARP - Neurogenic muscle weakness, ataxia and retinitis pigmentosa en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
626798015 Neurogenic muscle weakness, ataxia and retinitis pigmentosa (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
790971000052113 neurogen muskelsvaghet, ataxi och retinitis pigmentosa sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


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 Some
Neurogenic muscle weakness, ataxia and retinitis pigmentosa Occurrence Congenital true Inferred relationship Some 1
Neurogenic muscle weakness, ataxia and retinitis pigmentosa Finding site Body system structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

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