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Terminology chevron_right Concepts chevron_right 90036004

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Component

90036004

The component that hold information about this concept.

Fully Specified Name (FSN)

Vitelliform dystrophy (disorder)

Shortest Term

Best's disease

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

Vitelliform dystrophy (disorder)

SCTID: 90036004, Primitive, Inactive

90036004|Vitelliform dystrophy (disorder)|

en Vitelliform dystrophy
en Vitelliform dystrophy (disorder)
en Vitelliform macular dystrophy

Expression

90036004 |Vitelliform dystrophy (disorder)|
 <<< 

Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1235527018 - Best's disease (en) View
1235527018	en	Synonym (core metadata concept)	Best's disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	False
149249010 - Vitelliform dystrophy (en) View
149249010	en	Synonym (core metadata concept)	Vitelliform dystrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
833056010 - Vitelliform dystrophy (disorder) (en) View
833056010	en	Fully specified name (core metadata concept)	Vitelliform dystrophy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1235526010 - Vitelliform macular dystrophy (en) View
1235526010	en	Synonym (core metadata concept)	Vitelliform macular dystrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (295378027) - 90036004 -> 276436007 (116680003) View
116680003 \|Is a (attribute)\|	276436007 \|Hereditary macular dystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5049076020) - 90036004 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9224631023) - 90036004 -> 82859000 (363698007) View
363698007 \|Finding site (attribute)\|	82859000 \|Macula lutea structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12103889027) - 90036004 -> 247155003 (42752001) View
42752001 \|Due to (attribute)\|	247155003 \|Macular vitelliform deposits (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (295379024) - 90036004 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (900332027) - 90036004 -> 82859000 (363698007) View
363698007 \|Finding site (attribute)\|	82859000 \|Macula lutea structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5049077027) - 90036004 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

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

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 (bbef2e21-3e8a-5056-8271-1cd36cebcca5) 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)\|

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (295378027) - 90036004 -> 276436007 (116680003) View
116680003 \|Is a (attribute)\|	276436007 \|Hereditary macular dystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5049076020) - 90036004 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9224631023) - 90036004 -> 82859000 (363698007) View
363698007 \|Finding site (attribute)\|	82859000 \|Macula lutea structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12103889027) - 90036004 -> 247155003 (42752001) View
42752001 \|Due to (attribute)\|	247155003 \|Macular vitelliform deposits (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (295379024) - 90036004 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (900332027) - 90036004 -> 82859000 (363698007) View
363698007 \|Finding site (attribute)\|	82859000 \|Macula lutea structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5049077027) - 90036004 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

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