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Terminology chevron_right Concepts chevron_right 723450004

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Component

723450004

The component that hold information about this concept.

Fully Specified Name (FSN)

Pigmented paravenous retinochoroidal atrophy (disorder)

Shortest Term

Pigmented paravenous chorioretinal 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

Pigmented paravenous retinochoroidal atrophy (disorder)

SCTID: 723450004, Primitive, Active

723450004|Pigmented paravenous retinochoroidal atrophy (disorder)|

en Pigmented paravenous chorioretinal atrophy
en Pigmented paravenous retinochoroidal atrophy
en Pigmented paravenous retinochoroidal atrophy (disorder)
en Pprca - pigmented paravenous retinochoroidal atrophy

Expression

723450004 |Pigmented paravenous retinochoroidal atrophy (disorder)|
 <<< 95686007 |Chorioretinal atrophy (disorder)| + 
66091009 |Congenital disease (disorder)| + 
363343008 |Hereditary disorder of the visual system (disorder)|
        { 116676008 |Associated morphology (attribute)| = 13331008 |Atrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 13331008 |Atrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 68703001 |Choroidal structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3424670013 - Pigmented paravenous chorioretinal atrophy (en) View
3424670013	en	Synonym (core metadata concept)	Pigmented paravenous chorioretinal atrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3424669012 - Pigmented paravenous retinochoroidal atrophy (en) View
3424669012	en	Synonym (core metadata concept)	Pigmented paravenous retinochoroidal atrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3424668016 - Pigmented paravenous retinochoroidal atrophy (disorder) (en) View
3424668016	en	Fully specified name (core metadata concept)	Pigmented paravenous retinochoroidal atrophy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3424671012 - PPRCA - pigmented paravenous retinochoroidal atrophy (en) View
3424671012	en	Synonym (core metadata concept)	PPRCA - pigmented paravenous retinochoroidal atrophy	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6818204029) - 723450004 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6818205028) - 723450004 -> 95686007 (116680003) View
116680003 \|Is a (attribute)\|	95686007 \|Chorioretinal atrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6818206027) - 723450004 -> 363343008 (116680003) View
116680003 \|Is a (attribute)\|	363343008 \|Hereditary disorder of the visual system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6818207020) - 723450004 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6818208026) - 723450004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6818210029) - 723450004 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6818211025) - 723450004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6823142028) - 723450004 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6823143022) - 723450004 -> 68703001 (363698007) View
363698007 \|Finding site (attribute)\|	68703001 \|Choroidal structure (body structure)\|	3	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
66091009 View
66091009	Congenital disease (disorder)	Congenital disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363343008 View
363343008	Hereditary disorder of the visual system (disorder)	Hereditary disorder of the visual system	900000000000073002 \|Sufficiently defined by necessary conditions 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 (8e04a1dd-5ce2-560a-b4b0-5f2d44a92012) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H35.5	TRUE	ALWAYS H35.5 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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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