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Component

1259673008

The component that hold information about this concept.

Fully Specified Name (FSN)

Dementia due to neurofilament inclusion body disease (disorder)

Shortest Term

Dementia due to neurofilament inclusion body disease

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

Dementia due to neurofilament inclusion body disease (disorder)

SCTID: 1259673008, Primitive, Active

1259673008|Dementia due to neurofilament inclusion body disease (disorder)|

en Dementia due to neurofilament inclusion body disease
en Dementia due to neurofilament inclusion body disease (disorder)

Expression

1259673008 |Dementia due to neurofilament inclusion body disease (disorder)|
 <<< 230270009 |Frontotemporal dementia (disorder)| + 
192794001 |Cerebral degeneration associated with another disorder (disorder)| + 
724776007 |Dementia due to disorder of central nervous system (disorder)| : 
        { 363713009 |Has interpretation (attribute)| = 260379002 |Impaired (qualifier value)|,
363714003 |Interprets (attribute)| = 311465003 |Cognitive functions (observable entity)| }
        { 116676008 |Associated morphology (attribute)| = 107669003 |Degenerative abnormality (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 78277001 |Temporal lobe structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 107669003 |Degenerative abnormality (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 83251001 |Frontal lobe structure (body structure)| }
        { 42752001 |Due to (attribute)| = 23853001 |Disorder of the central nervous system (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
5158785018 - Dementia due to neurofilament inclusion body disease (en) View
5158785018	en	Synonym (core metadata concept)	Dementia due to neurofilament inclusion body disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5157577010 - Dementia due to neurofilament inclusion body disease (disorder) (en) View
5157577010	en	Fully specified name (core metadata concept)	Dementia due to neurofilament inclusion body disease (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15465064027) - 1259673008 -> 386806002 (116680003) View
116680003 \|Is a (attribute)\|	386806002 \|Impaired cognition (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15677652025) - 1259673008 -> 724776007 (116680003) View
116680003 \|Is a (attribute)\|	724776007 \|Dementia due to disorder of central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15465063022) - 1259673008 -> 230270009 (116680003) View
116680003 \|Is a (attribute)\|	230270009 \|Frontotemporal dementia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15465065026) - 1259673008 -> 311465003 (363714003) View
363714003 \|Interprets (attribute)\|	311465003 \|Cognitive functions (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15465066025) - 1259673008 -> 260379002 (363713009) View
363713009 \|Has interpretation (attribute)\|	260379002 \|Impaired (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15465067023) - 1259673008 -> 78277001 (363698007) View
363698007 \|Finding site (attribute)\|	78277001 \|Temporal lobe structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15465068029) - 1259673008 -> 107669003 (116676008) View
116676008 \|Associated morphology (attribute)\|	107669003 \|Degenerative abnormality (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15465069021) - 1259673008 -> 83251001 (363698007) View
363698007 \|Finding site (attribute)\|	83251001 \|Frontal lobe structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15465070022) - 1259673008 -> 107669003 (116676008) View
116676008 \|Associated morphology (attribute)\|	107669003 \|Degenerative abnormality (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15465154022) - 1259673008 -> 192794001 (116680003) View
116680003 \|Is a (attribute)\|	192794001 \|Cerebral degeneration associated with another disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15465835024) - 1259673008 -> 23853001 (42752001) View
42752001 \|Due to (attribute)\|	23853001 \|Disorder of the central nervous system (disorder)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
724776007 View
724776007	Dementia due to disorder of central nervous system (disorder)	Dementia due to disorder of central nervous system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
192794001 View
192794001	Cerebral degeneration associated with another disorder (disorder)	Cerebral degeneration in diseases ec	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
230270009 View
230270009	Frontotemporal dementia (disorder)	Picks disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

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 (59a74e42-9976-5158-ac96-efe9d1f3fb3e) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G31.9	TRUE	ALWAYS G31.9	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)\|
ExtendedMap object (fa144877-c74c-5b01-a009-38b3ffa6d194) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	F02.8	TRUE	ALWAYS F02.8 \| 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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