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Terminology chevron_right Concepts chevron_right 80328002

Production

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Component

80328002

The component that hold information about this concept.

Fully Specified Name (FSN)

Progressive cone-rod dystrophy (disorder)

Shortest Term

Cone-rod retinal 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

Progressive cone-rod dystrophy (disorder)

SCTID: 80328002, Primitive, Active

80328002|Progressive cone-rod dystrophy (disorder)|

en Cone-rod retinal dystrophy
en Progressive cone-rod dystrophy
en Progressive cone-rod dystrophy (disorder)

Expression

80328002 |Progressive cone-rod dystrophy (disorder)|
 <<< 128283000 |Chronic nervous system disorder (disorder)| + 
106018006 |Hereditary degenerative disease of central nervous system (disorder)| + 
41799005 |Hereditary retinal dystrophy (disorder)| + 
54767005 |Disorder of visual pathways (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 113324008 |Structure of neuroepithelial layer of retina (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
1234464015 - Cone-rod retinal dystrophy (en) View
1234464015	en	Synonym (core metadata concept)	Cone-rod retinal dystrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
133294010 - Progressive cone-rod dystrophy (en) View
133294010	en	Synonym (core metadata concept)	Progressive cone-rod dystrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
821476014 - Progressive cone-rod dystrophy (disorder) (en) View
821476014	en	Fully specified name (core metadata concept)	Progressive cone-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 (13908825029) - 80328002 -> 1899006 (116680003) View
116680003 \|Is a (attribute)\|	1899006 \|Autosomal hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5049200020) - 80328002 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12103800026) - 80328002 -> 106018006 (116680003) View
116680003 \|Is a (attribute)\|	106018006 \|Hereditary degenerative disease of central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12103801027) - 80328002 -> 128283000 (116680003) View
116680003 \|Is a (attribute)\|	128283000 \|Chronic nervous system disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12103802023) - 80328002 -> 54767005 (116680003) View
116680003 \|Is a (attribute)\|	54767005 \|Disorder of visual pathways (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12103803029) - 80328002 -> 255314001 (263502005) View
263502005 \|Clinical course (attribute)\|	255314001 \|Progressive (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12103804024) - 80328002 -> 113324008 (363698007) View
363698007 \|Finding site (attribute)\|	113324008 \|Structure of neuroepithelial layer of retina (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (874602026) - 80328002 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5049199022) - 80328002 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (278593024) - 80328002 -> 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
106018006 View
106018006	Hereditary degenerative disease of central nervous system (disorder)	Hereditary degenerative disease of central nervous system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
54767005 View
54767005	Disorder of visual pathways (disorder)	Disorder of visual pathways	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
41799005 View
41799005	Hereditary retinal dystrophy (disorder)	Hereditary retinal dystrophy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
128283000 View
128283000	Chronic nervous system disorder (disorder)	Chronic nervous system disease	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 (525fd54f-0389-56e9-9654-183dffa322bb) 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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