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Terminology chevron_right Concepts chevron_right 770791000

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Component

770791000

The component that hold information about this concept.

Fully Specified Name (FSN)

Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder)

Shortest Term

Autosomal dominant neovascular inflammatory vitreoretinopathy

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 neovascular inflammatory vitreoretinopathy (disorder)

SCTID: 770791000, Primitive, Active

770791000|Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder)|

en Autosomal dominant neovascular inflammatory vitreoretinopathy
en Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder)

Expression

770791000 |Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder)|
 <<< 247182006 |Vitreoretinal degeneration (disorder)| + 
363343008 |Hereditary disorder of the visual system (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| + 
128296004 |Chronic disease of ocular adnexa (disorder)| + 
363045008 |Connective tissue hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 13331008 |Atrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 47538007 |Vitreous body structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 13331008 |Atrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 264141008 |Peripheral retina (body structure)| }
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3702808018 - Autosomal dominant neovascular inflammatory vitreoretinopathy (en) View
3702808018	en	Synonym (core metadata concept)	Autosomal dominant neovascular inflammatory vitreoretinopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3702807011 - Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) (en) View
3702807011	en	Fully specified name (core metadata concept)	Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9635890026) - 770791000 -> 27624003 (116680003) View
116680003 \|Is a (attribute)\|	27624003 \|Chronic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9641457025) - 770791000 -> 33359002 (116676008) View
116676008 \|Associated morphology (attribute)\|	33359002 \|Degeneration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12094920020) - 770791000 -> 128296004 (116680003) View
116680003 \|Is a (attribute)\|	128296004 \|Chronic disease of ocular adnexa (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12094921024) - 770791000 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12094922028) - 770791000 -> 363045008 (116680003) View
116680003 \|Is a (attribute)\|	363045008 \|Connective tissue hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9635894024) - 770791000 -> 255314001 (263502005) View
263502005 \|Clinical course (attribute)\|	255314001 \|Progressive (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9635891027) - 770791000 -> 247182006 (116680003) View
116680003 \|Is a (attribute)\|	247182006 \|Vitreoretinal degeneration (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9635892023) - 770791000 -> 363343008 (116680003) View
116680003 \|Is a (attribute)\|	363343008 \|Hereditary disorder of the visual system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9635893029) - 770791000 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9641455022) - 770791000 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9641456023) - 770791000 -> 264141008 (363698007) View
363698007 \|Finding site (attribute)\|	264141008 \|Peripheral retina (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9641458024) - 770791000 -> 47538007 (363698007) View
363698007 \|Finding site (attribute)\|	47538007 \|Vitreous body structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
247182006 View
247182006	Vitreoretinal degeneration (disorder)	Vitreoretinal degeneration	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363045008 View
363045008	Connective tissue hereditary disorder (disorder)	Connective tissue hereditary disorder	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
128296004 View
128296004	Chronic disease of ocular adnexa (disorder)	Chronic disease of ocular adnexa	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 (c5c9bea6-459d-5ac2-97bd-61e52d2ee51f) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H35.2	TRUE	ALWAYS H35.2 \| 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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