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Terminology chevron_right Concepts chevron_right 702429008

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Component

702429008

The component that hold information about this concept.

Fully Specified Name (FSN)

Frontotemporal dementia with parkinsonism-17 (disorder)

Shortest Term

Familial pick's 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

Frontotemporal dementia with parkinsonism-17 (disorder)

SCTID: 702429008, Primitive, Active

702429008|Frontotemporal dementia with parkinsonism-17 (disorder)|

en Disinhibition-dementia-parkinsonism-amytrophy complex
en Frontotemporal dementia with parkinsonism-17
en Frontotemporal dementia with parkinsonism-17 (disorder)
en Familial pick's disease
en Ftdp-17 - frontotemporal dementia with parkinsonism 17
en Wilhelmsen-lynch disease

Expression

702429008 |Frontotemporal dementia with parkinsonism-17 (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
106018006 |Hereditary degenerative disease of central nervous system (disorder)| + 
230273006 |Frontotemporal degeneration (disorder)| + 
32798002 |Parkinsonism (disorder)| + 
52448006 |Dementia (disorder)| + 
897164004 |Structural abnormality of cerebral cortex (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 85775002 |Neurofibrillary degeneration (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 26972005 |Structure of cortex of frontal lobe (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 85775002 |Neurofibrillary degeneration (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 53464006 |Structure of cortex of temporal lobe (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 260379002 |Impaired (qualifier value)|,
363714003 |Interprets (attribute)| = 311465003 |Cognitive functions (observable entity)| }
        { 363698007 |Finding site (attribute)| = 32610002 |Basal ganglion structure (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 255361000 |Slow (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
2995445011 - Disinhibition-dementia-parkinsonism-amytrophy complex (en) View
2995445011	en	Synonym (core metadata concept)	Disinhibition-dementia-parkinsonism-amytrophy complex	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
2995187016 - Frontotemporal dementia with parkinsonism-17 (en) View
2995187016	en	Synonym (core metadata concept)	Frontotemporal dementia with parkinsonism-17	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2995675012 - Frontotemporal dementia with parkinsonism-17 (disorder) (en) View
2995675012	en	Fully specified name (core metadata concept)	Frontotemporal dementia with parkinsonism-17 (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2994998010 - Familial Pick's disease (en) View
2994998010	en	Synonym (core metadata concept)	Familial Pick's disease	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
2995742010 - FTDP-17 - Frontotemporal dementia with parkinsonism 17 (en) View
2995742010	en	Synonym (core metadata concept)	FTDP-17 - Frontotemporal dementia with parkinsonism 17	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
2995324015 - Wilhelmsen-Lynch disease (en) View
2995324015	en	Synonym (core metadata concept)	Wilhelmsen-Lynch disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16347145022) - 702429008 -> 128128003 (116680003) View
116680003 \|Is a (attribute)\|	128128003 \|Disorder of cerebral cortex (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16377365026) - 702429008 -> 897164004 (116680003) View
116680003 \|Is a (attribute)\|	897164004 \|Structural abnormality of cerebral cortex (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4968622021) - 702429008 -> 81308009 (116680003) View
116680003 \|Is a (attribute)\|	81308009 \|Disorder of brain (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4968623027) - 702429008 -> 60342002 (116680003) View
116680003 \|Is a (attribute)\|	60342002 \|Movement disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4968624022) - 702429008 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4968625023) - 702429008 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13882841024) - 702429008 -> 255324009 (363714003) View
363714003 \|Interprets (attribute)\|	255324009 \|Movement (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16346501022) - 702429008 -> 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 (16346502026) - 702429008 -> 230273006 (116680003) View
116680003 \|Is a (attribute)\|	230273006 \|Frontotemporal degeneration (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16346503020) - 702429008 -> 32798002 (116680003) View
116680003 \|Is a (attribute)\|	32798002 \|Parkinsonism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16346504025) - 702429008 -> 52448006 (116680003) View
116680003 \|Is a (attribute)\|	52448006 \|Dementia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16346505029) - 702429008 -> 32610002 (363698007) View
363698007 \|Finding site (attribute)\|	32610002 \|Basal ganglion structure (body structure)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16346508027) - 702429008 -> 311465003 (363714003) View
363714003 \|Interprets (attribute)\|	311465003 \|Cognitive functions (observable entity)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16346509024) - 702429008 -> 260379002 (363713009) View
363713009 \|Has interpretation (attribute)\|	260379002 \|Impaired (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16347146023) - 702429008 -> 26972005 (363698007) View
363698007 \|Finding site (attribute)\|	26972005 \|Structure of cortex of frontal lobe (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16347147025) - 702429008 -> 85775002 (116676008) View
116676008 \|Associated morphology (attribute)\|	85775002 \|Neurofibrillary degeneration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16347148024) - 702429008 -> 53464006 (363698007) View
363698007 \|Finding site (attribute)\|	53464006 \|Structure of cortex of temporal lobe (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16347149027) - 702429008 -> 85775002 (116676008) View
116676008 \|Associated morphology (attribute)\|	85775002 \|Neurofibrillary degeneration (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16354253024) - 702429008 -> 363847004 (363714003) View
363714003 \|Interprets (attribute)\|	363847004 \|Movement observable (observable entity)\|	6	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16354254029) - 702429008 -> 255361000 (363713009) View
363713009 \|Has interpretation (attribute)\|	255361000 \|Slow (qualifier value)\|	6	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4968621025) - 702429008 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
897164004 View
897164004	Structural abnormality of cerebral cortex (disorder)	Abnormal cerebral cortex morphology	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
230273006 View
230273006	Frontotemporal degeneration (disorder)	Lobar atrophy	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
32798002 View
32798002	Parkinsonism (disorder)	Parkinsonism	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

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1260328002 View
1260328002	Familial multiple system deposition of tau protein (disorder)	Familial multiple system tauopathy	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 (2cfd58de-87d7-5c82-8e36-2f156c37731e) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	F02.0	TRUE	ALWAYS F02.0 \| 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)\|
ExtendedMap object (80b6ee9e-b3ba-50ec-a892-df42f56b7825) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G31.0	TRUE	ALWAYS G31.0	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)\|

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