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Terminology chevron_right Concepts chevron_right 314407005

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Extended Map with ID “1ab00c3e-8d62-5e8a-848e-eabadd35dfe0” doesn’t exist. Perhaps it was deleted?

Component

314407005

The component that hold information about this concept.

Fully Specified Name (FSN)

Retinal dystrophy (disorder)

Shortest Term

Retinal 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

Retinal dystrophy (disorder)

SCTID: 314407005, Defined, Active

314407005|Retinal dystrophy (disorder)|

en Retinal dystrophy
en Retinal dystrophy (disorder)

Expression

314407005 |Retinal dystrophy (disorder)|
 === 95695004 |Degeneration of retina (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (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
458765013 - Retinal dystrophy (en) View
458765013	en	Synonym (core metadata concept)	Retinal dystrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
711209016 - Retinal dystrophy (disorder) (en) View
711209016	en	Fully specified name (core metadata concept)	Retinal dystrophy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (141709025) - 314407005 -> 29555009 (116680003) View
116680003 \|Is a (attribute)\|	29555009 \|Retinal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5049349026) - 314407005 -> 62585004 (116680003) View
116680003 \|Is a (attribute)\|	62585004 \|Degenerative disorder of eye (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12076918029) - 314407005 -> 95695004 (116680003) View
116680003 \|Is a (attribute)\|	95695004 \|Degeneration of retina (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (677803026) - 314407005 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5049350026) - 314407005 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5049351027) - 314407005 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	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
232049001 View
232049001	Adult vitelliform macular dystrophy (disorder)	Gass disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1187543005 View
1187543005	Dystrophy of retina due to gm2 gangliosidosis (disorder)	Retinal dystrophy due to gm2 gangliosidosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
763387005 View
763387005	Best vitelliform macular dystrophy (disorder)	Best disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
722437006 View
722437006	Ectopia lentis, chorioretinal dystrophy, myopia syndrome (disorder)	Ectopia lentis, chorioretinal dystrophy, myopia syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
40121000119107 View
40121000119107	Retinal dystrophy due to systemic disorder (disorder)	Retinal dystrophy due to systemic disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
35531000119107 View
35531000119107	Dystrophy of sensory retina (disorder)	Sensory retinal dystrophy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
342581000119102 View
342581000119102	Retinal pigment epithelial dystrophy (disorder)	Retinal pigment epithelial dystrophy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
41799005 View
41799005	Hereditary retinal dystrophy (disorder)	Hereditary retinal dystrophy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
236531005 View
236531005	Renal dysplasia and retinal aplasia (disorder)	Loken senior syndrome	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 (d65e9cb2-8013-54ae-9b8e-4695567aaed8) 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)\|

Terminology chevron_right Concepts chevron_right 314407005

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