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Terminology chevron_right Concepts chevron_right 231995008

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Component

231995008

The component that hold information about this concept.

Fully Specified Name (FSN)

Myopic chorioretinal atrophy (disorder)

Shortest Term

Peripheral myopic 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

Myopic chorioretinal atrophy (disorder)

SCTID: 231995008, Primitive, Active

231995008|Myopic chorioretinal atrophy (disorder)|

en Gross myopic retinal degeneration
en Myopic chorioretinal atrophy
en Myopic chorioretinal atrophy (disorder)
en Myopic chorioretinal degeneration
en Peripheral myopic atrophy

Expression

231995008 |Myopic chorioretinal atrophy (disorder)|
 <<< 95695004 |Degeneration of retina (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 107669003 |Degenerative abnormality (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
347626010 - Gross myopic retinal degeneration (en) View
347626010	en	Synonym (core metadata concept)	Gross myopic retinal degeneration	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
347624013 - Myopic chorioretinal atrophy (en) View
347624013	en	Synonym (core metadata concept)	Myopic chorioretinal atrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
620002011 - Myopic chorioretinal atrophy (disorder) (en) View
620002011	en	Fully specified name (core metadata concept)	Myopic chorioretinal atrophy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
347625014 - Myopic chorioretinal degeneration (en) View
347625014	en	Synonym (core metadata concept)	Myopic chorioretinal degeneration	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
347627018 - Peripheral myopic atrophy (en) View
347627018	en	Synonym (core metadata concept)	Peripheral myopic atrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (3431357025) - 231995008 -> 33359002 (116676008) View
116676008 \|Associated morphology (attribute)\|	33359002 \|Degeneration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12065694023) - 231995008 -> 107669003 (116676008) View
116676008 \|Associated morphology (attribute)\|	107669003 \|Degenerative abnormality (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (501845027) - 231995008 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (501846026) - 231995008 -> 33359002 (116676008) View
116676008 \|Associated morphology (attribute)\|	33359002 \|Degeneration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3431358024) - 231995008 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (43545023) - 231995008 -> 302893000 (116680003) View
116680003 \|Is a (attribute)\|	302893000 \|Chorioretinal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (43544022) - 231995008 -> 95695004 (116680003) View
116680003 \|Is a (attribute)\|	95695004 \|Degeneration of retina (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
95695004 View
95695004	Degeneration of retina (disorder)	Retinal degeneration	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 (ca93a9a3-a43c-567e-8b7f-13f30c16ab93) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H31.1	TRUE	ALWAYS H31.1	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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