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Terminology chevron_right Concepts chevron_right 40121000119107

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Component

40121000119107

The component that hold information about this concept.

Fully Specified Name (FSN)

Retinal dystrophy due to systemic disorder (disorder)

Shortest Term

Retinal dystrophy due to systemic disorder

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Retinal dystrophy due to systemic disorder (disorder)

SCTID: 40121000119107, Defined, Active

40121000119107|Retinal dystrophy due to systemic disorder (disorder)|

en Retinal dystrophy due to systemic disorder
en Retinal dystrophy due to systemic disorder (disorder)

Expression

40121000119107 |Retinal dystrophy due to systemic disorder (disorder)|
 === 314407005 |Retinal dystrophy (disorder)| : 
        { 42752001 |Due to (attribute)| = 56019007 |Systemic disease (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
3082466019 - Retinal dystrophy due to systemic disorder (en) View
3082466019	en	Synonym (core metadata concept)	Retinal dystrophy due to systemic disorder	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3082465015 - Retinal dystrophy due to systemic disorder (disorder) (en) View
3082465015	en	Fully specified name (core metadata concept)	Retinal dystrophy due to systemic disorder (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6270017025) - 40121000119107 -> 56019007 (42752001) View
42752001 \|Due to (attribute)\|	56019007 \|Systemic disease (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6270016023) - 40121000119107 -> 314407005 (116680003) View
116680003 \|Is a (attribute)\|	314407005 \|Retinal dystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6270018024) - 40121000119107 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6270019027) - 40121000119107 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
314407005 View
314407005	Retinal dystrophy (disorder)	Retinal dystrophy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1231663000 View
1231663000	Retinitis pigmentosa due to systemic disease (disorder)	Retinitis pigmentosa due to systemic disease	900000000000073002 \|Sufficiently defined by necessary conditions 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 (c5f97556-828a-534b-86f1-3a8ce15aa933) 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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