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Terminology chevron_right Concepts chevron_right 782822006

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Component

782822006

The component that hold information about this concept.

Fully Specified Name (FSN)

Infantile cerebellar and retinal degeneration (disorder)

Shortest Term

Infantile cerebellar and retinal degeneration

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

Infantile cerebellar and retinal degeneration (disorder)

SCTID: 782822006, Primitive, Active

782822006|Infantile cerebellar and retinal degeneration (disorder)|

en Infantile cerebellar and retinal degeneration
en Infantile cerebellar and retinal degeneration (disorder)

Expression

782822006 |Infantile cerebellar and retinal degeneration (disorder)|
 <<< 85995004 |Autosomal recessive hereditary disorder (disorder)| + 
95695004 |Degeneration of retina (disorder)| + 
26360005 |Hereditary optic atrophy (disorder)| + 
37650008 |Hereditary cerebellar degeneration (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 107669003 |Degenerative abnormality (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 113305005 |Cerebellar structure (body structure)|,
246454002 |Occurrence (attribute)| = 3658006 |Infancy (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 107669003 |Degenerative abnormality (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)|,
246454002 |Occurrence (attribute)| = 3658006 |Infancy (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 68616007 |Primary atrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 18234004 |Optic nerve structure (body structure)|,
246454002 |Occurrence (attribute)| = 3658006 |Infancy (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3756075011 - Infantile cerebellar and retinal degeneration (en) View
3756075011	en	Synonym (core metadata concept)	Infantile cerebellar and retinal degeneration	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3756074010 - Infantile cerebellar and retinal degeneration (disorder) (en) View
3756074010	en	Fully specified name (core metadata concept)	Infantile cerebellar and retinal degeneration (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (11227194024) - 782822006 -> 312942003 (116680003) View
116680003 \|Is a (attribute)\|	312942003 \|Inherited optic neuropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11227202024) - 782822006 -> 33359002 (116676008) View
116676008 \|Associated morphology (attribute)\|	33359002 \|Degeneration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11227203025) - 782822006 -> 33359002 (116676008) View
116676008 \|Associated morphology (attribute)\|	33359002 \|Degeneration (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12094571026) - 782822006 -> 107669003 (116676008) View
116676008 \|Associated morphology (attribute)\|	107669003 \|Degenerative abnormality (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12094572022) - 782822006 -> 107669003 (116676008) View
116676008 \|Associated morphology (attribute)\|	107669003 \|Degenerative abnormality (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11227190026) - 782822006 -> 95695004 (116680003) View
116680003 \|Is a (attribute)\|	95695004 \|Degeneration of retina (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11227191027) - 782822006 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11227192023) - 782822006 -> 3658006 (246454002) View
246454002 \|Occurrence (attribute)\|	3658006 \|Infancy (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11227193029) - 782822006 -> 113305005 (363698007) View
363698007 \|Finding site (attribute)\|	113305005 \|Cerebellar structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11227195020) - 782822006 -> 3658006 (246454002) View
246454002 \|Occurrence (attribute)\|	3658006 \|Infancy (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11227196021) - 782822006 -> 3658006 (246454002) View
246454002 \|Occurrence (attribute)\|	3658006 \|Infancy (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11227197028) - 782822006 -> 68616007 (116676008) View
116676008 \|Associated morphology (attribute)\|	68616007 \|Primary atrophy (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11227198022) - 782822006 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11227199025) - 782822006 -> 37650008 (116680003) View
116680003 \|Is a (attribute)\|	37650008 \|Hereditary cerebellar degeneration (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11227200027) - 782822006 -> 18234004 (363698007) View
363698007 \|Finding site (attribute)\|	18234004 \|Optic nerve structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11227201028) - 782822006 -> 26360005 (116680003) View
116680003 \|Is a (attribute)\|	26360005 \|Hereditary optic atrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
26360005 View
26360005	Hereditary optic atrophy (disorder)	Hereditary optic atrophy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
37650008 View
37650008	Hereditary cerebellar degeneration (disorder)	Hereditary cerebellar degeneration	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
95695004 View
95695004	Degeneration of retina (disorder)	Retinal degeneration	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 (ee81beb6-60cb-5028-83f8-cc612479fffd) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E88.8	TRUE	ALWAYS E88.8 \| 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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