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Terminology chevron_right Concepts chevron_right 1172584005

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Component

1172584005

The component that hold information about this concept.

Fully Specified Name (FSN)

Childhood-onset basal ganglia degeneration syndrome (disorder)

Shortest Term

Lenk ploski 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

Childhood-onset basal ganglia degeneration syndrome (disorder)

SCTID: 1172584005, Primitive, Active

1172584005|Childhood-onset basal ganglia degeneration syndrome (disorder)|

en Childhood-onset basal ganglia degeneration syndrome
en Childhood-onset basal ganglia degeneration syndrome (disorder)
en Lenk ploski syndrome

Expression

1172584005 |Childhood-onset basal ganglia degeneration syndrome (disorder)|
 <<< 106018006 |Hereditary degenerative disease of central nervous system (disorder)| + 
15802004 |Dystonia (disorder)| + 
2584003 |Cerebral degeneration in childhood (disorder)| + 
70835005 |Disorder of basal ganglia (disorder)| + 
78689005 |Chronic brain syndrome (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 107669003 |Degenerative abnormality (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 32610002 |Basal ganglion structure (body structure)|,
246454002 |Occurrence (attribute)| = 255398004 |Childhood (qualifier value)| }
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (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
4634472015 - Childhood-onset basal ganglia degeneration syndrome (en) View
4634472015	en	Synonym (core metadata concept)	Childhood-onset basal ganglia degeneration syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4634473013 - Childhood-onset basal ganglia degeneration syndrome (disorder) (en) View
4634473013	en	Fully specified name (core metadata concept)	Childhood-onset basal ganglia degeneration syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4634474019 - Lenk Ploski syndrome (en) View
4634474019	en	Synonym (core metadata concept)	Lenk Ploski syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (14008432028) - 1172584005 -> 255324009 (363714003) View
363714003 \|Interprets (attribute)\|	255324009 \|Movement (observable entity)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16350854026) - 1172584005 -> 363847004 (363714003) View
363714003 \|Interprets (attribute)\|	363847004 \|Movement observable (observable entity)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14008425021) - 1172584005 -> 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 (14008426022) - 1172584005 -> 15802004 (116680003) View
116680003 \|Is a (attribute)\|	15802004 \|Dystonia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14008427029) - 1172584005 -> 2584003 (116680003) View
116680003 \|Is a (attribute)\|	2584003 \|Cerebral degeneration in childhood (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14008428023) - 1172584005 -> 70835005 (116680003) View
116680003 \|Is a (attribute)\|	70835005 \|Disorder of basal ganglia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14008429026) - 1172584005 -> 78689005 (116680003) View
116680003 \|Is a (attribute)\|	78689005 \|Chronic brain syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14008430020) - 1172584005 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14008431024) - 1172584005 -> 255314001 (263502005) View
263502005 \|Clinical course (attribute)\|	255314001 \|Progressive (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14008433022) - 1172584005 -> 255398004 (246454002) View
246454002 \|Occurrence (attribute)\|	255398004 \|Childhood (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14008434027) - 1172584005 -> 32610002 (363698007) View
363698007 \|Finding site (attribute)\|	32610002 \|Basal ganglion structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14008435026) - 1172584005 -> 107669003 (116676008) View
116676008 \|Associated morphology (attribute)\|	107669003 \|Degenerative abnormality (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
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
2584003 View
2584003	Cerebral degeneration in childhood (disorder)	Cerebral degeneration in childhood	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
15802004 View
15802004	Dystonia (disorder)	Dystonia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
70835005 View
70835005	Disorder of basal ganglia (disorder)	Disease of basal ganglia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
78689005 View
78689005	Chronic brain syndrome (disorder)	Chronic brain syndrome	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	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 (ac1471bb-9983-5a79-8616-6bd3fa81890b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G31.8	TRUE	ALWAYS G31.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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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