237984008: Neurogenic muscle weakness, ataxia and retinitis pigmentosa (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Neurogenic muscle weakness, ataxia and retinitis pigmentosa
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Neurogenic muscle weakness, ataxia and retinitis pigmentosa
• \Congenital disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Neurogenic muscle weakness, ataxia and retinitis pigmentosa

Status: current, Primitive. 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	Active	Case insensitive	SNOMED CT core
356687018	NARP - Neurogenic muscle weakness, ataxia and retinitis pigmentosa	en	Synonym	Active	Case sensitive	SNOMED CT core
626798015	Neurogenic muscle weakness, ataxia and retinitis pigmentosa (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

REPLACED BY association reference set

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