30508001: Charcot-Marie-Tooth disease, type II (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 II	Is a	Charcot-Marie-Tooth disease	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Charcot-Marie-Tooth disease, type II	Associated morphology	Atrophy	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Charcot-Marie-Tooth disease, type II	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Charcot-Marie-Tooth disease, type II	Finding site	Nerve structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Charcot-Marie-Tooth disease, type II	Finding site	Peripheral nervous system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Charcot-Marie-Tooth disease, type II	Associated morphology	Neuropathic atrophy	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Charcot-Marie-Tooth disease, type II	Is a	Neuropathy	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Charcot-Marie-Tooth disease, type II	Associated morphology	Atrophy	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

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

POSSIBLY EQUIVALENT TO association reference set

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