dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 37650008

Production

add

Component

37650008

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary cerebellar degeneration (disorder)

Shortest Term

Hereditary cerebellar degeneration

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

Hereditary cerebellar degeneration (disorder)

SCTID: 37650008, Defined, Active

37650008|Hereditary cerebellar degeneration (disorder)|

en Hereditary cerebellar degeneration
en Hereditary cerebellar degeneration (disorder)

Expression

37650008 |Hereditary cerebellar degeneration (disorder)|
 === 95646004 |Cerebellar degeneration (disorder)| + 
106018006 |Hereditary degenerative disease of central nervous system (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 107669003 |Degenerative abnormality (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 113305005 |Cerebellar structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
62802011 - Hereditary cerebellar degeneration (en) View
62802011	en	Synonym (core metadata concept)	Hereditary cerebellar degeneration	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
769541014 - Hereditary cerebellar degeneration (disorder) (en) View
769541014	en	Fully specified name (core metadata concept)	Hereditary cerebellar degeneration (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (209201025) - 37650008 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3690627025) - 37650008 -> 33359002 (116676008) View
116676008 \|Associated morphology (attribute)\|	33359002 \|Degeneration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12080262029) - 37650008 -> 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 (12080263023) - 37650008 -> 107669003 (116676008) View
116676008 \|Associated morphology (attribute)\|	107669003 \|Degenerative abnormality (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3573335026) - 37650008 -> 223176004 (116680003) View
116680003 \|Is a (attribute)\|	223176004 \|Cerebellar disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3573336025) - 37650008 -> 52522001 (116680003) View
116680003 \|Is a (attribute)\|	52522001 \|Degenerative brain disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6545558026) - 37650008 -> 95646004 (116680003) View
116680003 \|Is a (attribute)\|	95646004 \|Cerebellar degeneration (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3421101023) - 37650008 -> 113305005 (363698007) View
363698007 \|Finding site (attribute)\|	113305005 \|Cerebellar structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3599157027) - 37650008 -> 33359002 (116676008) View
116676008 \|Associated morphology (attribute)\|	33359002 \|Degeneration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3613714027) - 37650008 -> 113305005 (363698007) View
363698007 \|Finding site (attribute)\|	113305005 \|Cerebellar structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (209200029) - 37650008 -> 23732000 (116680003) View
116680003 \|Is a (attribute)\|	23732000 \|Primary cerebellar degeneration (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3421102027) - 37650008 -> 44071007 (116676008) View
116676008 \|Associated morphology (attribute)\|	44071007 \|Primary degeneration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (766079024) - 37650008 -> 44071007 (116676008) View
116676008 \|Associated morphology (attribute)\|	44071007 \|Primary degeneration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (766082025) - 37650008 -> 113305005 (363698007) View
363698007 \|Finding site (attribute)\|	113305005 \|Cerebellar structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2227506029) - 37650008 -> 91502009 (116680003) View
116680003 \|Is a (attribute)\|	91502009 \|Spinocerebellar disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

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
95646004 View
95646004	Cerebellar degeneration (disorder)	Thoái hóa tiểu não	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1237514002 View
1237514002	Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome (disorder)	Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1237625002 View
1237625002	Autosomal recessive cerebellar ataxia due to cwf19 like cell cycle control factor 1 deficiency (disorder)	Scar17 - spinocerebellar ataxia autosomal recessive type 17	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1217381009 View
1217381009	Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome (disorder)	Gpaa1-related biosynthesis defect	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1208481000 View
1208481000	Progressive cerebello-cerebral atrophy (disorder)	Progressive cerebello-cerebral atrophy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1172696009 View
1172696009	Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome (disorder)	Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1172843003 View
1172843003	Combined oxidative phosphorylation defect type 29 (disorder)	Combined oxidative phosphorylation defect type 29	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
782737003 View
782737003	Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome (disorder)	Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
782822006 View
782822006	Infantile cerebellar and retinal degeneration (disorder)	Infantile cerebellar and retinal degeneration	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
770725000 View
770725000	Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly (disorder)	Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
770898002 View
770898002	Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to ww domain containing oxidoreductase deficiency (disorder)	Autosomal recessive spinocerebellar ataxia type 12	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
724283004 View
724283004	Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder)	H-abc - hypomyelination, atrophy of basal ganglia and cerebellum	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
722293005 View
722293005	Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome (disorder)	Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
699328003 View
699328003	Myoclonic epilepsy myopathy sensory ataxia (disorder)	Spinocerebellar ataxia with epilepsy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
10394003 View
10394003	Friedreich ataxia (disorder)	Familial ataxia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
129609000 View
129609000	Spinocerebellar ataxia (disorder)	Spinocerebellar ataxia	900000000000074008 \|Necessary but not sufficient concept 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 (efab0c25-b356-5517-9d4b-ab7a83f21d8a) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G11.9	TRUE	ALWAYS G11.9	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)\|

Terminology chevron_right Concepts chevron_right 37650008

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches