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Terminology chevron_right Concepts chevron_right 68222009

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Pigmentary retinal dystrophy (disorder)

Shortest Term

Lauber's disease

Definition Status

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Pigmentary retinal dystrophy (disorder)

SCTID: 68222009, Primitive, Inactive

68222009|Pigmentary retinal dystrophy (disorder)|

Expression

68222009 |Pigmentary retinal dystrophy (disorder)|
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Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
113323018 - Albipunctate retinal dystrophy (en) View
113323018	en	Synonym (core metadata concept)	Albipunctate retinal dystrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
113325013 - Fundus albipunctatus (en) View
113325013	en	Synonym (core metadata concept)	Fundus albipunctatus	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
113322011 - Pigmentary retinal dystrophy (en) View
113322011	en	Synonym (core metadata concept)	Pigmentary retinal dystrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
808034013 - Pigmentary retinal dystrophy (disorder) (en) View
808034013	en	Fully specified name (core metadata concept)	Pigmentary retinal dystrophy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
113324012 - Lauber's disease (en) View
113324012	en	Synonym (core metadata concept)	Lauber's disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (259047020) - 68222009 -> 41799005 (116680003) View
116680003 \|Is a (attribute)\|	41799005 \|Hereditary retinal dystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5049267020) - 68222009 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5049268026) - 68222009 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (844310027) - 68222009 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

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 (38c26501-8f07-579c-adf0-50a31c1afb60) 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)\|

Descriptions