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Terminology chevron_right Concepts chevron_right 15059000

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Component

15059000

The component that hold information about this concept.

Fully Specified Name (FSN)

Retinal dystrophy in systemic lipidosis (disorder)

Shortest Term

Retinal dystrophy in systemic lipidosis

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

Retinal dystrophy in systemic lipidosis (disorder)

SCTID: 15059000, Primitive, Active

15059000|Retinal dystrophy in systemic lipidosis (disorder)|

en Retinal dystrophy in systemic lipidosis
en Retinal dystrophy in systemic lipidosis (disorder)

Expression

15059000 |Retinal dystrophy in systemic lipidosis (disorder)|
 <<< 10741005 |Lipid storage disease (disorder)| + 
41799005 |Hereditary retinal dystrophy (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 5665001 |Retinal 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
25573016 - Retinal dystrophy in systemic lipidosis (en) View
25573016	en	Synonym (core metadata concept)	Retinal dystrophy in systemic lipidosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
741702016 - Retinal dystrophy in systemic lipidosis (disorder) (en) View
741702016	en	Fully specified name (core metadata concept)	Retinal dystrophy in systemic lipidosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (706580021) - 15059000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (706581020) - 15059000 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5049061028) - 15059000 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5049062024) - 15059000 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1669325026) - 15059000 -> 19416009 (116680003) View
116680003 \|Is a (attribute)\|	19416009 \|Congenital anomaly of eye (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (170406021) - 15059000 -> 87290003 (116680003) View
116680003 \|Is a (attribute)\|	87290003 \|Congenital anomaly of head (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (170405020) - 15059000 -> 10741005 (116680003) View
116680003 \|Is a (attribute)\|	10741005 \|Lipid storage disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (170407028) - 15059000 -> 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
10741005 View
10741005	Lipid storage disease (disorder)	Lipidoses	900000000000074008 \|Necessary but not sufficient concept 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

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 (8b9bd4fb-7c01-516c-b7a1-f80457ea70a9) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E75.6	TRUE	ALWAYS E75.6	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)\|
ExtendedMap object (a9ad4d78-9c80-53e9-bc3a-cfc2aca01cdb) 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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