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Terminology chevron_right Concepts chevron_right 770667002

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Component

770667002

The component that hold information about this concept.

Fully Specified Name (FSN)

Occult macular dystrophy (disorder)

Shortest Term

Occult macular dystrophy

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

Occult macular dystrophy (disorder)

SCTID: 770667002, Primitive, Active

770667002|Occult macular dystrophy (disorder)|

en Occult macular dystrophy
en Occult macular dystrophy (disorder)
en Ocmd - occult macular dystrophy
en Omd - occult macular dystrophy

Expression

770667002 |Occult macular dystrophy (disorder)|
 <<< 27624003 |Chronic disease (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| + 
276436007 |Hereditary macular dystrophy (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 82859000 |Macula lutea structure (body structure)| }
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3701927013 - Occult macular dystrophy (en) View
3701927013	en	Synonym (core metadata concept)	Occult macular dystrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3701926016 - Occult macular dystrophy (disorder) (en) View
3701926016	en	Fully specified name (core metadata concept)	Occult macular dystrophy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3701928015 - OCMD - occult macular dystrophy (en) View
3701928015	en	Synonym (core metadata concept)	OCMD - occult macular dystrophy	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3701929011 - OMD - occult macular dystrophy (en) View
3701929011	en	Synonym (core metadata concept)	OMD - occult macular dystrophy	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9621789025) - 770667002 -> 255314001 (263502005) View
263502005 \|Clinical course (attribute)\|	255314001 \|Progressive (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9621790023) - 770667002 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9621791022) - 770667002 -> 27624003 (116680003) View
116680003 \|Is a (attribute)\|	27624003 \|Chronic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9621792026) - 770667002 -> 82859000 (363698007) View
363698007 \|Finding site (attribute)\|	82859000 \|Macula lutea structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9621793020) - 770667002 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9621794025) - 770667002 -> 276436007 (116680003) View
116680003 \|Is a (attribute)\|	276436007 \|Hereditary macular dystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
27624003 View
27624003	Chronic disease (disorder)	Chronic disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
276436007 View
276436007	Hereditary macular dystrophy (disorder)	Macular dystrophy	900000000000074008 \|Necessary but not sufficient concept 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 (aeadb0a7-f2d5-5537-b8af-b4f0b63398f4) 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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