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Terminology chevron_right Concepts chevron_right 193158000

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Component

193158000

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary motor and sensory neuropathy (disorder)

Shortest Term

Peroneal muscular atrophy

Definition Status

900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Hereditary motor and sensory neuropathy (disorder)

SCTID: 193158000, Primitive, Inactive

193158000|Hereditary motor and sensory neuropathy (disorder)|

en Hereditary motor and sensory neuropathy
en Hereditary motor and sensory neuropathy (disorder)
en Hereditary peripheral neuropathy
en Peroneal muscular atrophy
en Charcot-marie-tooth disease
en Cmt - charcot-marie-tooth disease
en Hmsn - hereditary motor and sensory neuropathy
en Hsmn - hereditary sensory and motor neuropathy

Expression

193158000 |Hereditary motor and sensory neuropathy (disorder)|
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Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
297512013 - Hereditary motor and sensory neuropathy (en) View
297512013	en	Synonym (core metadata concept)	Hereditary motor and sensory neuropathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2710696012 - Hereditary motor and sensory neuropathy (disorder) (en) View
2710696012	en	Fully specified name (core metadata concept)	Hereditary motor and sensory neuropathy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
297516011 - Hereditary peripheral neuropathy (en) View
297516011	en	Synonym (core metadata concept)	Hereditary peripheral neuropathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
297515010 - Peroneal muscular atrophy (en) View
297515010	en	Synonym (core metadata concept)	Peroneal muscular atrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
577014019 - Hereditary motor and sensory neuropathy (en) View
577014019	en	Fully specified name (core metadata concept)	Hereditary motor and sensory neuropathy	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
297518012 - Charcot-Marie-Tooth disease (en) View
297518012	en	Synonym (core metadata concept)	Charcot-Marie-Tooth disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
297513015 - CMT - Charcot-Marie-Tooth disease (en) View
297513015	en	Synonym (core metadata concept)	CMT - Charcot-Marie-Tooth disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
297514014 - HMSN - Hereditary motor and sensory neuropathy (en) View
297514014	en	Synonym (core metadata concept)	HMSN - Hereditary motor and sensory neuropathy	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
297517019 - HSMN - Hereditary sensory and motor neuropathy (en) View
297517019	en	Synonym (core metadata concept)	HSMN - Hereditary sensory and motor neuropathy	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help

Terminology chevron_right Concepts chevron_right 193158000

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