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Terminology chevron_right Concepts chevron_right 421506003

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Component

421506003

The component that hold information about this concept.

Fully Specified Name (FSN)

Retinal pigment epithelium atrophy (disorder)

Shortest Term

Rpe atrophy

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

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

Summary

Retinal pigment epithelium atrophy (disorder)

SCTID: 421506003, Defined, Active

421506003|Retinal pigment epithelium atrophy (disorder)|

en Retinal pigment epithelium atrophy
en Retinal pigment epithelium atrophy (disorder)
en Rpe atrophy

Expression

421506003 |Retinal pigment epithelium atrophy (disorder)|
 === 421689001 |Retinal pigment epithelial abnormality (disorder)| + 
405722004 |Atrophic retina (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 13331008 |Atrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 41275009 |Structure of retinal pigment epithelium (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2618525013 - Retinal pigment epithelium atrophy (en) View
2618525013	en	Synonym (core metadata concept)	Retinal pigment epithelium atrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2639108016 - Retinal pigment epithelium atrophy (disorder) (en) View
2639108016	en	Fully specified name (core metadata concept)	Retinal pigment epithelium atrophy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2615841019 - Retinal pigment epithelium atrophy (finding) (en) View
2615841019	en	Fully specified name (core metadata concept)	Retinal pigment epithelium atrophy (finding)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
2623223018 - RPE atrophy (en) View
2623223018	en	Synonym (core metadata concept)	RPE atrophy	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (3071156022) - 421506003 -> 41275009 (363698007) View
363698007 \|Finding site (attribute)\|	41275009 \|Structure of retinal pigment epithelium (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3071157029) - 421506003 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3365665023) - 421506003 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3448618024) - 421506003 -> 41275009 (363698007) View
363698007 \|Finding site (attribute)\|	41275009 \|Structure of retinal pigment epithelium (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2954912028) - 421506003 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3012627022) - 421506003 -> 405722004 (116680003) View
116680003 \|Is a (attribute)\|	405722004 \|Atrophic retina (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2946922028) - 421506003 -> 421689001 (116680003) View
116680003 \|Is a (attribute)\|	421689001 \|Retinal pigment epithelial abnormality (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
421689001 View
421689001	Retinal pigment epithelial abnormality (disorder)	Rpe changes	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

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
1142279005 View
1142279005	Patchy atrophy of retinal pigment epithelium (disorder)	Patchy atrophy of retinal pigment epithelium	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 (306fac98-8141-56c4-8e0a-fcfda504b8f4) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H35.8	TRUE	ALWAYS H35.8	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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