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Terminology chevron_right Concepts chevron_right 725392005

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Component

725392005

The component that hold information about this concept.

Fully Specified Name (FSN)

Autosomal dominant striatal neurodegeneration (disorder)

Shortest Term

Autosomal dominant striatal neurodegeneration

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

Autosomal dominant striatal neurodegeneration (disorder)

SCTID: 725392005, Primitive, Active

725392005|Autosomal dominant striatal neurodegeneration (disorder)|

en Adsd - autosomal dominant striatal neurodegeneration
en Autosomal dominant striatal neurodegeneration
en Autosomal dominant striatal neurodegeneration (disorder)

Expression

725392005 |Autosomal dominant striatal neurodegeneration (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
32798002 |Parkinsonism (disorder)| + 
418143002 |Cerebral degeneration (disorder)| + 
106018006 |Hereditary degenerative disease of central nervous system (disorder)| + 
896882009 |Structural abnormality of corpus striatum (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 107669003 |Degenerative abnormality (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 31428008 |Corpus striatum 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
3441980015 - ADSD - autosomal dominant striatal neurodegeneration (en) View
3441980015	en	Synonym (core metadata concept)	ADSD - autosomal dominant striatal neurodegeneration	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3441979018 - Autosomal dominant striatal neurodegeneration (en) View
3441979018	en	Synonym (core metadata concept)	Autosomal dominant striatal neurodegeneration	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3441978014 - Autosomal dominant striatal neurodegeneration (disorder) (en) View
3441978014	en	Fully specified name (core metadata concept)	Autosomal dominant striatal neurodegeneration (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16377390029) - 725392005 -> 896882009 (116680003) View
116680003 \|Is a (attribute)\|	896882009 \|Structural abnormality of corpus striatum (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13882611020) - 725392005 -> 255324009 (363714003) View
363714003 \|Interprets (attribute)\|	255324009 \|Movement (observable entity)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13882612029) - 725392005 -> 255361000 (363713009) View
363713009 \|Has interpretation (attribute)\|	255361000 \|Slow (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16350750026) - 725392005 -> 363847004 (363714003) View
363714003 \|Interprets (attribute)\|	363847004 \|Movement observable (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16350751027) - 725392005 -> 255361000 (363713009) View
363713009 \|Has interpretation (attribute)\|	255361000 \|Slow (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6892485029) - 725392005 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6892487021) - 725392005 -> 33359002 (116676008) View
116676008 \|Associated morphology (attribute)\|	33359002 \|Degeneration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12091953027) - 725392005 -> 107669003 (116676008) View
116676008 \|Associated morphology (attribute)\|	107669003 \|Degenerative abnormality (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12091954022) - 725392005 -> 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 (6892483020) - 725392005 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6892484025) - 725392005 -> 32798002 (116680003) View
116680003 \|Is a (attribute)\|	32798002 \|Parkinsonism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6892486028) - 725392005 -> 418143002 (116680003) View
116680003 \|Is a (attribute)\|	418143002 \|Cerebral degeneration (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6892488027) - 725392005 -> 31428008 (363698007) View
363698007 \|Finding site (attribute)\|	31428008 \|Corpus striatum structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
896882009 View
896882009	Structural abnormality of corpus striatum (disorder)	Abnormal corpus striatum 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
418143002 View
418143002	Cerebral degeneration (disorder)	Cerebral degeneration	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

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 (9e3783f4-4ffb-5834-9da4-028189f4e4ec) 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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