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Terminology chevron_right Concepts chevron_right 50548001

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Component

50548001

The component that hold information about this concept.

Fully Specified Name (FSN)

Charcot-marie-tooth disease (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

Charcot-marie-tooth disease (disorder)

SCTID: 50548001, Primitive, Inactive

50548001|Charcot-marie-tooth disease (disorder)|

en Peroneal muscular atrophy
en Charcot-marie-tooth disease (disorder)
en Charcot-marie-tooth disease
en Cmt - charcot-marie-tooth disease

Expression

50548001 |Charcot-marie-tooth disease (disorder)|
 <<< 

Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
84200019 - Peroneal muscular atrophy (en) View
84200019	en	Synonym (core metadata concept)	Peroneal muscular atrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
788348015 - Charcot-Marie-Tooth disease (disorder) (en) View
788348015	en	Fully specified name (core metadata concept)	Charcot-Marie-Tooth disease (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
84201015 - Charcot-Marie-Tooth disease (en) View
84201015	en	Synonym (core metadata concept)	Charcot-Marie-Tooth disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
495705018 - CMT - Charcot-Marie-Tooth disease (en) View
495705018	en	Synonym (core metadata concept)	CMT - Charcot-Marie-Tooth disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
84203017 - Hereditary sensory-motor neuropathy, NOS (en) View
84203017	en	Synonym (core metadata concept)	Hereditary sensory-motor neuropathy, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
84202010 - Neuropathic muscular atrophy (en) View
84202010	en	Synonym (core metadata concept)	Neuropathic muscular atrophy	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (230244020) - 50548001 -> 88092000 (116680003) View
116680003 \|Is a (attribute)\|	88092000 \|Muscle atrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (230245021) - 50548001 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (798099028) - 50548001 -> 3058005 (363698007) View
363698007 \|Finding site (attribute)\|	3058005 \|Peripheral nervous system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1676751028) - 50548001 -> 257277002 (116680003) View
116680003 \|Is a (attribute)\|	257277002 \|Combined disorder of muscle and peripheral nerve (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2228732024) - 50548001 -> 398100001 (116680003) View
116680003 \|Is a (attribute)\|	398100001 \|Hereditary motor and sensory neuropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3393283027) - 50548001 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3393284022) - 50548001 -> 52996001 (116676008) View
116676008 \|Associated morphology (attribute)\|	52996001 \|Neuropathic atrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (798100020) - 50548001 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (798102028) - 50548001 -> 52996001 (116676008) View
116676008 \|Associated morphology (attribute)\|	52996001 \|Neuropathic atrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (230246022) - 50548001 -> 128202008 (116680003) View
116680003 \|Is a (attribute)\|	128202008 \|Hereditary motor and sensory neuropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (798101024) - 50548001 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

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
ExtendedMap object (589c2e46-d944-51a9-96c0-e09dbf59e761) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G60.0	TRUE	ALWAYS G60.0	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447637006 \|Map source concept is properly classified (foundation metadata concept)\|

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (230244020) - 50548001 -> 88092000 (116680003) View
116680003 \|Is a (attribute)\|	88092000 \|Muscle atrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (230245021) - 50548001 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (798099028) - 50548001 -> 3058005 (363698007) View
363698007 \|Finding site (attribute)\|	3058005 \|Peripheral nervous system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1676751028) - 50548001 -> 257277002 (116680003) View
116680003 \|Is a (attribute)\|	257277002 \|Combined disorder of muscle and peripheral nerve (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2228732024) - 50548001 -> 398100001 (116680003) View
116680003 \|Is a (attribute)\|	398100001 \|Hereditary motor and sensory neuropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3393283027) - 50548001 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3393284022) - 50548001 -> 52996001 (116676008) View
116676008 \|Associated morphology (attribute)\|	52996001 \|Neuropathic atrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (798100020) - 50548001 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (798102028) - 50548001 -> 52996001 (116676008) View
116676008 \|Associated morphology (attribute)\|	52996001 \|Neuropathic atrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (230246022) - 50548001 -> 128202008 (116680003) View
116680003 \|Is a (attribute)\|	128202008 \|Hereditary motor and sensory neuropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (798101024) - 50548001 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

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