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Terminology chevron_right Concepts chevron_right 232062002

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Component

232062002

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary vitreoretinopathy (disorder)

Shortest Term

Hereditary 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

Hereditary vitreoretinopathy (disorder)

SCTID: 232062002, Primitive, Active

232062002|Hereditary vitreoretinopathy (disorder)|

en Hereditary vitreoretinopathy
en Hereditary vitreoretinopathy (disorder)

Expression

232062002 |Hereditary vitreoretinopathy (disorder)|
 <<< 76682005 |Disorder of vitreous body (disorder)| + 
29555009 |Retinal disorder (disorder)| + 
363343008 |Hereditary disorder of the visual system (disorder)| + 
363045008 |Connective tissue hereditary disorder (disorder)| : 
        { 363698007 |Finding site (attribute)| = 47538007 |Vitreous body structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
347713018 - Hereditary vitreoretinopathy (en) View
347713018	en	Synonym (core metadata concept)	Hereditary vitreoretinopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
620078011 - Hereditary vitreoretinopathy (disorder) (en) View
620078011	en	Fully specified name (core metadata concept)	Hereditary vitreoretinopathy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (12065705022) - 232062002 -> 363045008 (116680003) View
116680003 \|Is a (attribute)\|	363045008 \|Connective tissue hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (502194026) - 232062002 -> 47538007 (363698007) View
363698007 \|Finding site (attribute)\|	47538007 \|Vitreous body structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3020916027) - 232062002 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2991690026) - 232062002 -> 399625000 (116680003) View
116680003 \|Is a (attribute)\|	399625000 \|Retinopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6572764021) - 232062002 -> 29555009 (116680003) View
116680003 \|Is a (attribute)\|	29555009 \|Retinal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6572765022) - 232062002 -> 363343008 (116680003) View
116680003 \|Is a (attribute)\|	363343008 \|Hereditary disorder of the visual system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (43638027) - 232062002 -> 76682005 (116680003) View
116680003 \|Is a (attribute)\|	76682005 \|Disorder of vitreous body (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
363045008 View
363045008	Connective tissue hereditary disorder (disorder)	Connective tissue hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
29555009 View
29555009	Retinal disorder (disorder)	Retinopathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
76682005 View
76682005	Disorder of vitreous body (disorder)	Vitreous disorder	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
1003309003 View
1003309003	Erosive vitreoretinopathy (disorder)	Erosive vitreoretinopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
78675000 View
78675000	Stickler syndrome (disorder)	Stickler syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
232063007 View
232063007	Familial exudative vitreoretinopathy (disorder)	Familial exudative vitreoretinopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
232064001 View
232064001	Wagner syndrome (disorder)	Wagner syndrome	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 (3856fc6a-127c-50dc-a938-648c5dcf7e4c) 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)\|

Terminology chevron_right Concepts chevron_right 232062002

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