52647008: Charcot-Marie-Tooth disease, type I (disorder)

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
198400014	Peroneal muscular atrophy of demyelinating type	en	Synonym	Active	Case insensitive	SNOMED CT core
496390011	Hereditary motor and sensory neuropathy type I	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
496391010	Hereditary sensory and autonomic neuropathy, type I	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
496392015	Dominant hereditary sensory neuropathy, type I	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
496393013	Acrodystrophic neuropathy	en	Synonym	Active	Case insensitive	SNOMED CT core
496394019	Charcot-Marie-Tooth disease of demyelinating type	en	Synonym	Active	Case sensitive	SNOMED CT core
790679010	Charcot-Marie-Tooth disease, type I (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core
87618018	Charcot-Marie-Tooth disease, type I	en	Synonym	Active	Case sensitive	SNOMED CT core
87619014	Hereditary sensory-motor neuropathy, type I	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
87620015	Inherited dominant hypertrophic neuropathy	en	Synonym	Active	Case insensitive	SNOMED CT core
87621016	HSMN, type I	en	Synonym	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian dialect reference set

Concept inactivation indicator reference set

Description inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set

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