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Terminology chevron_right Concepts chevron_right 95702003

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Component

95702003

The component that hold information about this concept.

Fully Specified Name (FSN)

Central progressive retinal atrophy (disorder)

Shortest Term

Central progressive retinal atrophy

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

Central progressive retinal atrophy (disorder)

SCTID: 95702003, Primitive, Active

95702003|Central progressive retinal atrophy (disorder)|

en Central progressive retinal atrophy
en Central progressive retinal atrophy (disorder)

Expression

95702003 |Central progressive retinal atrophy (disorder)|
 <<< 405722004 |Atrophic retina (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 13331008 |Atrophy (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
158536015 - Central progressive retinal atrophy (en) View
158536015	en	Synonym (core metadata concept)	Central progressive retinal atrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
839912018 - Central progressive retinal atrophy (disorder) (en) View
839912018	en	Fully specified name (core metadata concept)	Central progressive retinal atrophy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (930676026) - 95702003 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (930677024) - 95702003 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3409676023) - 95702003 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3464964027) - 95702003 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (307697024) - 95702003 -> 95704002 (116680003) View
116680003 \|Is a (attribute)\|	95704002 \|Retina atrophic (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2464347021) - 95702003 -> 405722004 (116680003) View
116680003 \|Is a (attribute)\|	405722004 \|Atrophic retina (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

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

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (e148b325-108d-5bc2-aca8-d7ba2f1df45c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H35.3	TRUE	ALWAYS H35.3 \| POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE	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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