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Terminology chevron_right Concepts chevron_right 719455002

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Component

719455002

The component that hold information about this concept.

Fully Specified Name (FSN)

Cone dystrophy with supernormal rod response (disorder)

Shortest Term

Cone dystrophy with supernormal rod response

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

Cone dystrophy with supernormal rod response (disorder)

SCTID: 719455002, Primitive, Active

719455002|Cone dystrophy with supernormal rod response (disorder)|

en Cone dystrophy with supernormal rod electroretinogram
en Cone dystrophy with supernormal rod response
en Cone dystrophy with supernormal rod response (disorder)

Expression

719455002 |Cone dystrophy with supernormal rod response (disorder)|
 <<< 85995004 |Autosomal recessive hereditary disorder (disorder)| + 
312917007 |Cone dystrophy (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 67540009 |Cone of retina (cell structure)| }
        { 363698007 |Finding site (attribute)| = 17139002 |Rod of retina (cell)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3316426010 - Cone dystrophy with supernormal rod electroretinogram (en) View
3316426010	en	Synonym (core metadata concept)	Cone dystrophy with supernormal rod electroretinogram	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3316425014 - Cone dystrophy with supernormal rod response (en) View
3316425014	en	Synonym (core metadata concept)	Cone dystrophy with supernormal rod response	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3316424013 - Cone dystrophy with supernormal rod response (disorder) (en) View
3316424013	en	Fully specified name (core metadata concept)	Cone dystrophy with supernormal rod response (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6628890023) - 719455002 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12091010029) - 719455002 -> 67540009 (363698007) View
363698007 \|Finding site (attribute)\|	67540009 \|Cone of retina (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12091011025) - 719455002 -> 17139002 (363698007) View
363698007 \|Finding site (attribute)\|	17139002 \|Rod of retina (cell)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6628887028) - 719455002 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6628888022) - 719455002 -> 312917007 (116680003) View
116680003 \|Is a (attribute)\|	312917007 \|Cone dystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6628889025) - 719455002 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
312917007 View
312917007	Cone dystrophy (disorder)	Cone dystrophy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	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 (bf437589-217b-57d9-9eea-e3fe0efc74f3) 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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