dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 314467007

Production

add

Component

314467007

The component that hold information about this concept.

Fully Specified Name (FSN)

Gyrate atrophy (disorder)

Shortest Term

Gyrate 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

Gyrate atrophy (disorder)

SCTID: 314467007, Primitive, Active

314467007|Gyrate atrophy (disorder)|

en Gyrate atrophy
en Gyrate atrophy (disorder)
en Gyrate atrophy of choroid and retina

Expression

314467007 |Gyrate atrophy (disorder)|
 <<< 95686007 |Chorioretinal atrophy (disorder)| + 
410053003 |Clinical manifestation of enzyme deficiency (disorder)| : 
        { 42752001 |Due to (attribute)| = 276426004 |Ornithine oxo-acid aminotransferase deficiency (disorder)| }
        { 116676008 |Associated morphology (attribute)| = 13331008 |Atrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 13331008 |Atrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 68703001 |Choroidal structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
458831015 - Gyrate atrophy (en) View
458831015	en	Synonym (core metadata concept)	Gyrate atrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
711275011 - Gyrate atrophy (disorder) (en) View
711275011	en	Fully specified name (core metadata concept)	Gyrate atrophy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
458832010 - Gyrate atrophy of choroid and retina (en) View
458832010	en	Synonym (core metadata concept)	Gyrate atrophy of choroid and retina	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
458833017 - Gyrate atrophy of the choroid AND/OR retina (en) View
458833017	en	Synonym (core metadata concept)	Gyrate atrophy of the choroid AND/OR retina	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2586414027) - 314467007 -> 276426004 (42752001) View
42752001 \|Due to (attribute)\|	276426004 \|Ornithine oxo-acid aminotransferase deficiency (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3343728022) - 314467007 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3343729025) - 314467007 -> 68703001 (363698007) View
363698007 \|Finding site (attribute)\|	68703001 \|Choroidal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3343730024) - 314467007 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6143529022) - 314467007 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6143531029) - 314467007 -> 68703001 (363698007) View
363698007 \|Finding site (attribute)\|	68703001 \|Choroidal structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6818105023) - 314467007 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6818106024) - 314467007 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1984797020) - 314467007 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1984799023) - 314467007 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1984800022) - 314467007 -> 68703001 (363698007) View
363698007 \|Finding site (attribute)\|	68703001 \|Choroidal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1984801021) - 314467007 -> 276426004 (363715002) View
363715002 \|Associated etiologic finding (attribute)\|	276426004 \|Ornithine oxo-acid aminotransferase deficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2539927020) - 314467007 -> 410053003 (116680003) View
116680003 \|Is a (attribute)\|	410053003 \|Clinical manifestation of enzyme deficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (141796025) - 314467007 -> 302893000 (116680003) View
116680003 \|Is a (attribute)\|	302893000 \|Chorioretinal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (677961028) - 314467007 -> 303295006 (363698007) View
363698007 \|Finding site (attribute)\|	303295006 \|Choroidal and/or retinal structures (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1984798026) - 314467007 -> 95686007 (116680003) View
116680003 \|Is a (attribute)\|	95686007 \|Chorioretinal atrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
95686007 View
95686007	Chorioretinal atrophy (disorder)	Chorioretinal atrophy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
410053003 View
410053003	Clinical manifestation of enzyme deficiency (disorder)	Clinical manifestation of enzyme deficiency	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 (5f9b6091-9b10-5f3c-9bfc-f4962445911d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H31.2	TRUE	ALWAYS H31.2	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)\|
ExtendedMap object (9f1e633a-f5d2-545d-9cd6-b92bd0d41c77) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H32.8	TRUE	ALWAYS H32.8	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)\|
ExtendedMap object (e3c10bba-7f61-5151-8d20-5230e6718eec) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q15.8	TRUE	ALWAYS Q15.8	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 314467007

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches