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Terminology chevron_right Concepts chevron_right 192794001

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Component

192794001

The component that hold information about this concept.

Fully Specified Name (FSN)

Cerebral degeneration associated with another disorder (disorder)

Shortest Term

Cerebral degeneration in diseases ec

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

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

Summary

Cerebral degeneration associated with another disorder (disorder)

SCTID: 192794001, Defined, Active

192794001|Cerebral degeneration associated with another disorder (disorder)|

en Cerebral degeneration associated with another disorder
en Cerebral degeneration associated with another disorder (disorder)

Expression

192794001 |Cerebral degeneration associated with another disorder (disorder)|
 === 418143002 |Cerebral degeneration (disorder)| + 
87536007 |Central nervous system complication (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 107669003 |Degenerative abnormality (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 83678007 |Cerebral structure (body structure)| }
        { 47429007 |Associated with (attribute)| = 64572001 |Disease (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2575727019 - Cerebral degeneration associated with another disorder (en) View
2575727019	en	Synonym (core metadata concept)	Cerebral degeneration associated with another disorder	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2562259015 - Cerebral degeneration associated with another disorder (disorder) (en) View
2562259015	en	Fully specified name (core metadata concept)	Cerebral degeneration associated with another disorder (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
296993015 - Cerebral degeneration in diseases EC (en) View
296993015	en	Synonym (core metadata concept)	Cerebral degeneration in diseases EC	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
576613015 - Cerebral degeneration in diseases EC (disorder) (en) View
576613015	en	Fully specified name (core metadata concept)	Cerebral degeneration in diseases EC (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13951514028) - 192794001 -> 87536007 (116680003) View
116680003 \|Is a (attribute)\|	87536007 \|Central nervous system complication (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3399994029) - 192794001 -> 33359002 (116676008) View
116676008 \|Associated morphology (attribute)\|	33359002 \|Degeneration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12067145020) - 192794001 -> 107669003 (116676008) View
116676008 \|Associated morphology (attribute)\|	107669003 \|Degenerative abnormality (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2874913022) - 192794001 -> 64572001 (47429007) View
47429007 \|Associated with (attribute)\|	64572001 \|Disease (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (960442020) - 192794001 -> 33359002 (116676008) View
116676008 \|Associated morphology (attribute)\|	33359002 \|Degeneration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1789477027) - 192794001 -> 83678007 (363698007) View
363698007 \|Finding site (attribute)\|	83678007 \|Cerebral structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3399995028) - 192794001 -> 83678007 (363698007) View
363698007 \|Finding site (attribute)\|	83678007 \|Cerebral structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (326570020) - 192794001 -> 192780002 (116680003) View
116680003 \|Is a (attribute)\|	192780002 \|Cerebral degenerations usually manifest in childhood (navigational concept)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1789478021) - 192794001 -> 255398004 (246454002) View
246454002 \|Occurrence (attribute)\|	255398004 \|Childhood (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2845361022) - 192794001 -> 418143002 (116680003) View
116680003 \|Is a (attribute)\|	418143002 \|Cerebral degeneration (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (960440028) - 192794001 -> 21483005 (363698007) View
363698007 \|Finding site (attribute)\|	21483005 \|Structure of central nervous system (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (960441029) - 192794001 -> 86522006 (363698007) View
363698007 \|Finding site (attribute)\|	86522006 \|Structure of telencephalon (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
87536007 View
87536007	Central nervous system complication (disorder)	Central nervous system complication	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
418143002 View
418143002	Cerebral degeneration (disorder)	Cerebral degeneration	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1260324000 View
1260324000	White matter disease due to anti-phospholipid syndrome (disorder)	White matter disease due to anti-phospholipid syndrome	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1260352009 View
1260352009	Frontotemporal dementia due to tardbp mutation (disorder)	Frontotemporal dementia due to tardbp mutation	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1260353004 View
1260353004	Frontotemporal dementia due to vcp mutation (disorder)	Frontotemporal dementia due to vcp mutation	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1260354005 View
1260354005	Frontotemporal dementia due to c9orf72 mutation (disorder)	Frontotemporal dementia due to c9orf72 mutation	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1260355006 View
1260355006	Frontotemporal dementia due to fus mutation (disorder)	Frontotemporal dementia due to fus mutation	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1259673008 View
1259673008	Dementia due to neurofilament inclusion body disease (disorder)	Dementia due to neurofilament inclusion body disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
230295005 View
230295005	Parkinsonism with calcification of basal ganglia (disorder)	Parkinsonism with calcification of basal ganglia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
359686005 View
359686005	Van bogaert's sclerosing leukoencephalitis (disorder)	Van bogaert sclerosing leucoencephalitis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
724565006 View
724565006	White matter disorder due to nutritional deficiency (disorder)	White matter disorder due to nutritional deficiency	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
192819000 View
192819000	Cerebral degeneration due to progressive multifocal leukoencephalopathy (disorder)	Cerebral degeneration due to progressive multifocal leucoencephalopathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
135761000119101 View
135761000119101	Cerebral degeneration due to alcoholism (disorder)	Cerebral degeneration due to alcoholism	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
135781000119105 View
135781000119105	Cerebral degeneration due to hypothyroidism (disorder)	Cerebral degeneration due to hypothyroidism	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
21921000119103 View
21921000119103	Dementia co-occurrent and due to pick's disease (disorder)	Dementia due to pick disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
192796004 View
192796004	Cerebral degeneration in mucopolysaccharidosis (disorder)	Cerebral degeneration in mucopolysaccharidosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
438513002 View
438513002	Cerebral degeneration due to parkinson's disease (disorder)	Cerebral degeneration due to parkinson disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
192791009 View
192791009	Cerebral degeneration in gaucher's disease (disorder)	Cerebral degeneration in gaucher disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
192813004 View
192813004	Cerebral degeneration due to cerebrovascular disease (disorder)	Cerebral degeneration due to cerebrovascular disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
192814005 View
192814005	Cerebral degeneration due to congenital hydrocephalus (disorder)	Cerebral degeneration due to congenital hydrocephalus	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
192815006 View
192815006	Cerebral degeneration due to neoplastic disease (disorder)	Cerebral degeneration due to neoplastic disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
192818008 View
192818008	Cerebral degeneration due to creutzfeldt-jakob disease (disorder)	Cerebral degeneration due to creutzfeldt-jakob disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
420146005 View
420146005	Cerebral degeneration associated with generalized lipidosis (disorder)	Cerebral degeneration in lipidoses	900000000000073002 \|Sufficiently defined by necessary conditions 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 (4807254c-c5a3-55a0-a6dd-5c5fa2108f84) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|
ExtendedMap object (f139f2c2-15bd-5142-8513-ee064795ecb2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G32.8	TRUE	ALWAYS G32.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION \| THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE	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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