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Terminology chevron_right Concepts chevron_right 702376003

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Component

702376003

The component that hold information about this concept.

Fully Specified Name (FSN)

Huntington disease-like syndrome (disorder)

Shortest Term

Huntington disease-like syndrome

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 disease-like syndrome (disorder)

SCTID: 702376003, Primitive, Active

702376003|Huntington disease-like syndrome (disorder)|

en Huntington disease-like syndrome
en Huntington disease-like syndrome (disorder)
en Huntington disease-like syndrome disorder
en Huntington disease phenocopy syndrome

Expression

702376003 |Huntington disease-like syndrome (disorder)|
 <<< 271700006 |Chorea (disorder)| : 
        { 363698007 |Finding site (attribute)| = 32610002 |Basal ganglion structure (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3038744019 - Huntington disease-like syndrome (en) View
3038744019	en	Synonym (core metadata concept)	Huntington disease-like syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3038760015 - Huntington disease-like syndrome (disorder) (en) View
3038760015	en	Fully specified name (core metadata concept)	Huntington disease-like syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
2995592013 - Huntington disease-like syndrome disorder (disorder) (en) View
2995592013	en	Fully specified name (core metadata concept)	Huntington disease-like syndrome disorder (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	False
2995278018 - Huntington disease-like syndrome disorder (en) View
2995278018	en	Synonym (core metadata concept)	Huntington disease-like syndrome disorder	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
2995145018 - Huntington disease phenocopy syndrome (en) View
2995145018	en	Synonym (core metadata concept)	Huntington disease phenocopy syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15512969022) - 702376003 -> 255324009 (363714003) View
363714003 \|Interprets (attribute)\|	255324009 \|Movement (observable entity)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6759826025) - 702376003 -> 70835005 (116680003) View
116680003 \|Is a (attribute)\|	70835005 \|Disorder of basal ganglia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6759827023) - 702376003 -> 76349003 (116680003) View
116680003 \|Is a (attribute)\|	76349003 \|Extrapyramidal disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6759828029) - 702376003 -> 230298007 (116680003) View
116680003 \|Is a (attribute)\|	230298007 \|Disorder presenting primarily with chorea (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13882838026) - 702376003 -> 255324009 (363714003) View
363714003 \|Interprets (attribute)\|	255324009 \|Movement (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15502042025) - 702376003 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15502230026) - 702376003 -> 271700006 (116680003) View
116680003 \|Is a (attribute)\|	271700006 \|Chorea (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15512970023) - 702376003 -> 363847004 (363714003) View
363714003 \|Interprets (attribute)\|	363847004 \|Movement observable (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6759829021) - 702376003 -> 32610002 (363698007) View
363698007 \|Finding site (attribute)\|	32610002 \|Basal ganglion structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4968260024) - 702376003 -> 37650008 (116680003) View
116680003 \|Is a (attribute)\|	37650008 \|Hereditary cerebellar degeneration (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4968261023) - 702376003 -> 33359002 (116676008) View
116676008 \|Associated morphology (attribute)\|	33359002 \|Degeneration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4968262027) - 702376003 -> 113305005 (363698007) View
363698007 \|Finding site (attribute)\|	113305005 \|Cerebellar structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
271700006 View
271700006	Chorea (disorder)	Chorea	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
724764007 View
724764007	Chorea co-occurrent and due to huntington disease-like condition (disorder)	Chorea with huntington disease-like condition	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
782743001 View
782743001	Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions (disorder)	C9orf72-related huntington disease phenocopy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
784371009 View
784371009	Huntington disease-like 1 (disorder)	Huntington disease-like 1	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
770939009 View
770939009	Huntington disease-like 3 (disorder)	Huntington disease-like 3	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
721228006 View
721228006	Huntington disease-like 2 (disorder)	Huntington disease-like 2	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 (46316d47-5f84-51f0-982c-866496f7aec3) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G11.9	TRUE	ALWAYS G11.9	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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