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Terminology chevron_right Concepts chevron_right 79556007

Production

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Component

79556007

The component that hold information about this concept.

Fully Specified Name (FSN)

Vitreoretinal dystrophy (disorder)

Shortest Term

Vitreoretinal dystrophy

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

Vitreoretinal dystrophy (disorder)

SCTID: 79556007, Primitive, Active

79556007|Vitreoretinal dystrophy (disorder)|

en Vitreoretinal dystrophy
en Vitreoretinal dystrophy (disorder)

Expression

79556007 |Vitreoretinal dystrophy (disorder)|
 <<< 41799005 |Hereditary retinal dystrophy (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
131985018 - Vitreoretinal dystrophy (en) View
131985018	en	Synonym (core metadata concept)	Vitreoretinal dystrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
820619014 - Vitreoretinal dystrophy (disorder) (en) View
820619014	en	Fully specified name (core metadata concept)	Vitreoretinal dystrophy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (872701027) - 79556007 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5049322026) - 79556007 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5049323020) - 79556007 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (277371026) - 79556007 -> 41799005 (116680003) View
116680003 \|Is a (attribute)\|	41799005 \|Hereditary retinal dystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
41799005 View
41799005	Hereditary retinal dystrophy (disorder)	Hereditary retinal dystrophy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
232065000 View
232065000	Goldmann-favre syndrome (disorder)	Goldmann-favre 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 (9d3b6444-a51a-58fd-814d-bf68c56f9174) 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 79556007

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