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Terminology chevron_right Concepts chevron_right 783203003

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Component

783203003

The component that hold information about this concept.

Fully Specified Name (FSN)

Ataxia with tapetoretinal degeneration syndrome (disorder)

Shortest Term

Ataxia with tapetoretinal degeneration 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

Ataxia with tapetoretinal degeneration syndrome (disorder)

SCTID: 783203003, Primitive, Active

783203003|Ataxia with tapetoretinal degeneration syndrome (disorder)|

en Ataxia with tapetoretinal degeneration syndrome
en Ataxia with tapetoretinal degeneration syndrome (disorder)

Expression

783203003 |Ataxia with tapetoretinal degeneration syndrome (disorder)|
 <<< 405722004 |Atrophic retina (disorder)| + 
61536007 |Peripheral retinal degeneration (disorder)| + 
85102008 |Cerebellar ataxia (disorder)| + 
247177004 |Chorioretinal degeneration (disorder)| + 
363343008 |Hereditary disorder of the visual system (disorder)| + 
763597000 |Hereditary ataxia (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 13331008 |Atrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 264141008 |Peripheral retina (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 107669003 |Degenerative abnormality (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 68703001 |Choroidal structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 113305005 |Cerebellar structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3758081011 - Ataxia with tapetoretinal degeneration syndrome (en) View
3758081011	en	Synonym (core metadata concept)	Ataxia with tapetoretinal degeneration syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3758082016 - Ataxia with tapetoretinal degeneration syndrome (disorder) (en) View
3758082016	en	Fully specified name (core metadata concept)	Ataxia with tapetoretinal degeneration syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (11281171024) - 783203003 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11569491020) - 783203003 -> 33359002 (116676008) View
116676008 \|Associated morphology (attribute)\|	33359002 \|Degeneration (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11569492029) - 783203003 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12094627021) - 783203003 -> 68703001 (363698007) View
363698007 \|Finding site (attribute)\|	68703001 \|Choroidal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12094628027) - 783203003 -> 405722004 (116680003) View
116680003 \|Is a (attribute)\|	405722004 \|Atrophic retina (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12094629024) - 783203003 -> 61536007 (116680003) View
116680003 \|Is a (attribute)\|	61536007 \|Peripheral retinal degeneration (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12094630025) - 783203003 -> 107669003 (116676008) View
116676008 \|Associated morphology (attribute)\|	107669003 \|Degenerative abnormality (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11281163020) - 783203003 -> 363343008 (116680003) View
116680003 \|Is a (attribute)\|	363343008 \|Hereditary disorder of the visual system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11281165029) - 783203003 -> 763597000 (116680003) View
116680003 \|Is a (attribute)\|	763597000 \|Hereditary ataxia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11281169024) - 783203003 -> 85102008 (116680003) View
116680003 \|Is a (attribute)\|	85102008 \|Cerebellar ataxia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11281170020) - 783203003 -> 247177004 (116680003) View
116680003 \|Is a (attribute)\|	247177004 \|Chorioretinal degeneration (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11569489028) - 783203003 -> 264141008 (363698007) View
363698007 \|Finding site (attribute)\|	264141008 \|Peripheral retina (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11569490021) - 783203003 -> 113305005 (363698007) View
363698007 \|Finding site (attribute)\|	113305005 \|Cerebellar structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11569493023) - 783203003 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
247177004 View
247177004	Chorioretinal degeneration (disorder)	Chorioretinal degeneration	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85102008 View
85102008	Cerebellar ataxia (disorder)	Cerebellar ataxia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
763597000 View
763597000	Hereditary ataxia (disorder)	Hereditary ataxia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
61536007 View
61536007	Peripheral retinal degeneration (disorder)	Thoái hóa võng mạc ngoại biên	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
405722004 View
405722004	Atrophic retina (disorder)	Atrophic retina	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363343008 View
363343008	Hereditary disorder of the visual system (disorder)	Hereditary disorder of the visual system	900000000000073002 \|Sufficiently defined by necessary conditions 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 (657f1010-3404-5b6e-bfea-359de0b95ef1) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G11.9	TRUE	ALWAYS G11.9 \| 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)\|
ExtendedMap object (cbe6bd15-4a9d-520f-b090-eb6469f826c2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H35.5	TRUE	ALWAYS H35.5	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 (ea7ad061-182d-58e5-b661-835b978abf77) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G11.1	TRUE	ALWAYS G11.1 \| 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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