30508001: Charcot-Marie-Tooth disease, type II (disorder)

Status: retired, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
484605018	Charcot-Marie-Tooth disease of neuronal type	en	Synonym	Active	Case sensitive	SNOMED CT core
484606017	Autosomal recessive sensory neuropathy	en	Synonym	Active	Case insensitive	SNOMED CT core
484607014	Dominant hereditary sensory neuropathy, type II	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
484608016	Hereditary sensory and autonomic neuropathy type II	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
484609012	Peroneal muscular atrophy of neuronal type	en	Synonym	Active	Case insensitive	SNOMED CT core
484610019	Painless whitlow disease	en	Synonym	Active	Case insensitive	SNOMED CT core
484611015	Hereditary sensory and autonomic neuropathy, type II	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
484612010	Hereditary motor and sensory neuropathy type II	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
51056015	Charcot-Marie-Tooth disease, type II	en	Synonym	Active	Case sensitive	SNOMED CT core
51057012	Hereditary sensory-motor neuropathy, type II	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
51058019	Inherited neuronal peroneal muscular atrophy	en	Synonym	Active	Case insensitive	SNOMED CT core
761520018	Charcot-Marie-Tooth disease, type II (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set

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