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Terminology chevron_right Concepts chevron_right 312917007

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Component

312917007

The component that hold information about this concept.

Fully Specified Name (FSN)

Cone dystrophy (disorder)

Shortest Term

Cone dystrophy

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

Cone dystrophy (disorder)

SCTID: 312917007, Defined, Active

312917007|Cone dystrophy (disorder)|

en Cone dystrophy
en Cone dystrophy (disorder)

Expression

312917007 |Cone dystrophy (disorder)|
 === 41799005 |Hereditary retinal dystrophy (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 67540009 |Cone of retina (cell structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
456725016 - Cone dystrophy (en) View
456725016	en	Synonym (core metadata concept)	Cone dystrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
709642015 - Cone dystrophy (disorder) (en) View
709642015	en	Fully specified name (core metadata concept)	Cone dystrophy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (5049117023) - 312917007 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12078971024) - 312917007 -> 67540009 (363698007) View
363698007 \|Finding site (attribute)\|	67540009 \|Cone of retina (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (675727022) - 312917007 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5049116025) - 312917007 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (140469022) - 312917007 -> 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
789676005 View
789676005	Blue cone monochromatism (disorder)	Cone monochromatism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
724000006 View
724000006	Retinohepatoendocrinologic syndrome (disorder)	Rhe syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
719455002 View
719455002	Cone dystrophy with supernormal rod response (disorder)	Cone dystrophy with supernormal rod response	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
56852002 View
56852002	Achromatopsia (disorder)	Achromatism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
267613004 View
267613004	Progressive cone dystrophy (without rod involvement) (disorder)	Progressive cone dystrophy (without rod involvement)	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 (67d1c93f-1fd1-57c2-bd42-cd3beb50d8e1) 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)\|

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