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

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Charcot-Marie-Tooth disease, type I	Is a	Charcot-Marie-Tooth disease	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Charcot-Marie-Tooth disease, type I	Associated morphology	Atrophy	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Charcot-Marie-Tooth disease, type I	Associated morphology	Neuropathic atrophy	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Charcot-Marie-Tooth disease, type I	Finding site	Nerve structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Charcot-Marie-Tooth disease, type I	Finding site	Peripheral nervous system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Charcot-Marie-Tooth disease, type I	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Charcot-Marie-Tooth disease, type I	Is a	Neuropathy	false	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Charcot-Marie-Tooth disease, type IA	Is a	False	Charcot-Marie-Tooth disease, type I	Inferred relationship	Existential restriction modifier (core metadata concept)
Charcot-Marie-Tooth disease, type IC (disorder)	Is a	False	Charcot-Marie-Tooth disease, type I	Inferred relationship	Existential restriction modifier (core metadata concept)
Charcot-Marie-Tooth disease, type IB	Is a	False	Charcot-Marie-Tooth disease, type I	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

GB English

US English

POSSIBLY EQUIVALENT TO association reference set

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