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Terminology chevron_right Concepts chevron_right 313003009

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Component

313003009

The component that hold information about this concept.

Fully Specified Name (FSN)

Rod dystrophy (disorder)

Shortest Term

Rod 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

Rod dystrophy (disorder)

SCTID: 313003009, Primitive, Active

313003009|Rod dystrophy (disorder)|

en Rod dystrophy
en Rod dystrophy (disorder)

Expression

313003009 |Rod dystrophy (disorder)|
 <<< 41799005 |Hereditary retinal dystrophy (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
456828014 - Rod dystrophy (en) View
456828014	en	Synonym (core metadata concept)	Rod dystrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
709738011 - Rod dystrophy (disorder) (en) View
709738011	en	Fully specified name (core metadata concept)	Rod dystrophy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (676052023) - 313003009 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5049343025) - 313003009 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5049344020) - 313003009 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (140582028) - 313003009 -> 41799005 (116680003) View
116680003 \|Is a (attribute)\|	41799005 \|Hereditary retinal dystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
41799005 View
41799005	Hereditary retinal dystrophy (disorder)	Hereditary retinal dystrophy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
232056007 View
232056007	Progressive rod dystrophy (disorder)	Progressive rod dystrophy	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 (2508823c-a4ba-5db4-98d3-a508e415018c) 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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