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Terminology chevron_right Concepts chevron_right 58756001

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Extended Map with ID “9d6969e8-eaa5-58da-b993-2c96464d8aab” doesn’t exist. Perhaps it was deleted?

Component

58756001

The component that hold information about this concept.

Fully Specified Name (FSN)

Huntington's chorea (disorder)

Shortest Term

Huntington chorea

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

Huntington's chorea (disorder)

SCTID: 58756001, Primitive, Active

58756001|Huntington's chorea (disorder)|

vi Múa giật huntington
en Huntington disease
en Huntington's disease
en Chronic progressive chorea
en Chronic progressive hereditary chorea
en Huntington chorea
en Hc - huntington chorea
en Hd - huntington chorea
en Huntington's chorea (disorder)
en Huntington's chorea

Expression

58756001 |Huntington's chorea (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
52448006 |Dementia (disorder)| + 
425919003 |Chronic organic mental disorder (disorder)| + 
257277002 |Combined disorder of muscle and peripheral nerve (disorder)| + 
363212003 |Hereditary disorder of musculoskeletal system (disorder)| + 
128237006 |Chronic disease of musculoskeletal system (disorder)| + 
15802004 |Dystonia (disorder)| + 
106018006 |Hereditary degenerative disease of central nervous system (disorder)| + 
271700006 |Chorea (disorder)| + 
1144383006 |Atrophy of caudate nucleus (disorder)| : 
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
        { 116676008 |Associated morphology (attribute)| = 13331008 |Atrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 11000004 |Caudate nucleus structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 3058005 |Peripheral nervous system structure (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 260379002 |Impaired (qualifier value)|,
363714003 |Interprets (attribute)| = 311465003 |Cognitive functions (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
480101000003111 - múa giật Huntington (vi) View
480101000003111	vi	Synonym (core metadata concept)	múa giật Huntington	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4024764019 - Huntington disease (en) View
4024764019	en	Synonym (core metadata concept)	Huntington disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
4024765018 - Huntington's disease (en) View
4024765018	en	Synonym (core metadata concept)	Huntington's disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
97643010 - Chronic progressive chorea (en) View
97643010	en	Synonym (core metadata concept)	Chronic progressive chorea	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
97644016 - Chronic progressive hereditary chorea (en) View
97644016	en	Synonym (core metadata concept)	Chronic progressive hereditary chorea	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
2838433019 - Huntington chorea (en) View
2838433019	en	Synonym (core metadata concept)	Huntington chorea	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
1231875011 - HC - Huntington chorea (en) View
1231875011	en	Synonym (core metadata concept)	HC - Huntington chorea	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
1231876012 - HD - Huntington chorea (en) View
1231876012	en	Synonym (core metadata concept)	HD - Huntington chorea	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
797523018 - Huntington's chorea (disorder) (en) View
797523018	en	Fully specified name (core metadata concept)	Huntington's chorea (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
97642017 - Huntington's chorea (en) View
97642017	en	Synonym (core metadata concept)	Huntington's chorea	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15512914024) - 58756001 -> 255324009 (363714003) View
363714003 \|Interprets (attribute)\|	255324009 \|Movement (observable entity)\|	7	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12933021021) - 58756001 -> 278849000 (116680003) View
116680003 \|Is a (attribute)\|	278849000 \|Cerebral atrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16299003028) - 58756001 -> 1144383006 (116680003) View
116680003 \|Is a (attribute)\|	1144383006 \|Atrophy of caudate nucleus (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (243638025) - 58756001 -> 230298007 (116680003) View
116680003 \|Is a (attribute)\|	230298007 \|Disorder presenting primarily with chorea (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (243639022) - 58756001 -> 70835005 (116680003) View
116680003 \|Is a (attribute)\|	70835005 \|Disorder of basal ganglia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12933022025) - 58756001 -> 255324009 (363714003) View
363714003 \|Interprets (attribute)\|	255324009 \|Movement (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15502010020) - 58756001 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15512915020) - 58756001 -> 363847004 (363714003) View
363714003 \|Interprets (attribute)\|	363847004 \|Movement observable (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (819947028) - 58756001 -> 32610002 (363698007) View
363698007 \|Finding site (attribute)\|	32610002 \|Basal ganglion structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2548923026) - 58756001 -> 76349003 (116680003) View
116680003 \|Is a (attribute)\|	76349003 \|Extrapyramidal disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11567016028) - 58756001 -> 78689005 (116680003) View
116680003 \|Is a (attribute)\|	78689005 \|Chronic brain syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11567017021) - 58756001 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12932986022) - 58756001 -> 52448006 (116680003) View
116680003 \|Is a (attribute)\|	52448006 \|Dementia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12932987029) - 58756001 -> 425919003 (116680003) View
116680003 \|Is a (attribute)\|	425919003 \|Chronic organic mental disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12932988023) - 58756001 -> 257277002 (116680003) View
116680003 \|Is a (attribute)\|	257277002 \|Combined disorder of muscle and peripheral nerve (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12932989026) - 58756001 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12932990024) - 58756001 -> 128237006 (116680003) View
116680003 \|Is a (attribute)\|	128237006 \|Chronic disease of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12932993021) - 58756001 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12932994026) - 58756001 -> 3058005 (363698007) View
363698007 \|Finding site (attribute)\|	3058005 \|Peripheral nervous system structure (body structure)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12932995025) - 58756001 -> 260379002 (363713009) View
363713009 \|Has interpretation (attribute)\|	260379002 \|Impaired (qualifier value)\|	6	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12932996029) - 58756001 -> 311465003 (363714003) View
363714003 \|Interprets (attribute)\|	311465003 \|Cognitive functions (observable entity)\|	6	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12933018024) - 58756001 -> 15802004 (116680003) View
116680003 \|Is a (attribute)\|	15802004 \|Dystonia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12933019027) - 58756001 -> 106018006 (116680003) View
116680003 \|Is a (attribute)\|	106018006 \|Hereditary degenerative disease of central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12933020022) - 58756001 -> 271700006 (116680003) View
116680003 \|Is a (attribute)\|	271700006 \|Chorea (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12933023024) - 58756001 -> 11000004 (363698007) View
363698007 \|Finding site (attribute)\|	11000004 \|Caudate nucleus structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12933024029) - 58756001 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11567015029) - 58756001 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11570465029) - 58756001 -> 255314001 (263502005) View
263502005 \|Clinical course (attribute)\|	255314001 \|Progressive (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1144383006 View
1144383006	Atrophy of caudate nucleus (disorder)	Atrophy of caudate nucleus	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
106018006 View
106018006	Hereditary degenerative disease of central nervous system (disorder)	Hereditary degenerative disease of central nervous system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
425919003 View
425919003	Chronic organic mental disorder (disorder)	Chronic organic brain syndrome	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
257277002 View
257277002	Combined disorder of muscle and peripheral nerve (disorder)	Myoneural disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
15802004 View
15802004	Dystonia (disorder)	Dystonia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
52448006 View
52448006	Dementia (disorder)	Dementia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
128237006 View
128237006	Chronic disease of musculoskeletal system (disorder)	Chronic musculoskeletal disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
271700006 View
271700006	Chorea (disorder)	Chorea	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363212003 View
363212003	Hereditary disorder of musculoskeletal system (disorder)	Hereditary disorder of musculoskeletal system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
230299004 View
230299004	Juvenile onset huntington's disease (disorder)	Juvenile onset huntington disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
230300007 View
230300007	Late onset huntington's disease (disorder)	Late onset huntington disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
230301006 View
230301006	Akinetic-rigid form of huntington's disease (disorder)	Akinetic-rigid form of huntington disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (859db5b6-5da0-54f0-9693-be616039fafa) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G10	TRUE	ALWAYS G10	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)\|

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