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113305005: Cerebellar structure (body structure)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
187142017 Cerebellum en Synonym Active Entire term case insensitive SNOMED CT core module
382977010 Cerebellar structure en Synonym Active Entire term case insensitive SNOMED CT core module
648477018 Cerebellar structure (body structure) en Fully specified name Active Entire term case insensitive SNOMED CT core module

170 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cerebellar structure Is a Infratentorial brain structure false Inferred relationship Existential restriction modifier
Cerebellar structure Is a Extrapyramidal system structure true Inferred relationship Existential restriction modifier
Cerebellar structure Is a Hindbrain structure false Inferred relationship Existential restriction modifier
Cerebellar structure Part of Entire infratentorial brain false Additional relationship Existential restriction modifier
Cerebellar structure Part of Entire extrapyramidal system false Additional relationship Existential restriction modifier
Cerebellar structure Is a Infratentorial brain part true Inferred relationship Existential restriction modifier
Cerebellar structure Is a Brain tissue structure true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Myoclonus, cerebellar ataxia, deafness syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 4
Spastic paraplegia, glaucoma, intellectual disability syndrome Finding site False Cerebellar structure Inferred relationship Existential restriction modifier 4
Spastic paraplegia, nephritis, deafness syndrome Finding site False Cerebellar structure Inferred relationship Existential restriction modifier 8
Spinocerebellar ataxia type 40 Finding site False Cerebellar structure Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 38 Finding site False Cerebellar structure Inferred relationship Existential restriction modifier 2
Sporadic adult-onset ataxia of unknown etiology Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Liponeurocytoma of cerebellum Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome Finding site False Cerebellar structure Inferred relationship Existential restriction modifier 4
Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Autosomal recessive cerebellar ataxia with late-onset spasticity Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Spectrin-associated autosomal recessive cerebellar ataxia Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Dentatorubropallidoluysian degeneration Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Fragile X associated tremor ataxia syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Chorea co-occurrent and due to dentatorubropallidoluysian degeneration Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 3
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia with axonal neuropathy type 1 Finding site False Cerebellar structure Inferred relationship Existential restriction modifier 2
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Finding site False Cerebellar structure Inferred relationship Existential restriction modifier 2
Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
X-linked non progressive cerebellar ataxia Finding site False Cerebellar structure Inferred relationship Existential restriction modifier 1
Ataxia pancytopenia syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 5
Leukoencephalopathy with mild cerebellar ataxia and white matter edema Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 3
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly Finding site False Cerebellar structure Inferred relationship Existential restriction modifier 2
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Autosomal recessive cerebelloparenchymal disorder type 3 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type C Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 4 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia dysmorphism syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 3
Congenital pontocerebellar hypoplasia type 2 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Cerebellar ataxia co-occurrent with ectodermal dysplasia Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 3
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Chudley McCullough syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 9 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Autosomal recessive cerebellar ataxia due to STIP1 homology and U-box containing protein 1 deficiency Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Infantile cerebellar and retinal degeneration Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Recessive mitochondrial ataxia syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Autosomal recessive cerebellar ataxia, psychomotor delay syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Congenital muscular dystrophy with cerebellar involvement Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Arnold Chiari type 2 without hydrocephalus Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Chiari malformation type IV Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Chiari malformation type II Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Capra DeMarco syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 3
Hydrocephalus due to Arnold Chiari malformation type 2 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Chiari malformation type I Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Closed spina bifida with Arnold-Chiari malformation Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 3
Chiari malformation Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Adult-onset autosomal recessive cerebellar ataxia Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Infantile-onset autosomal recessive non progressive cerebellar ataxia Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Ataxia with tapetoretinal degeneration syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 3
Congenital pontocerebellar hypoplasia type 10 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Gemignani syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 3
Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic ataxia with leukoencephalopathy Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Perinatal subependymal hemorrhage with intraventricular and intracerebral extension Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Saldino-Mainzer dysplasia Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 4
Hindbrain structure Is a True Cerebellar structure Inferred relationship Existential restriction modifier
Myoclonic epilepsy myopathy sensory ataxia Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 34 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 4
X-linked sideroblastic anemia with spinocerebellar ataxia Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 5
Spinocerebellar degeneration and corneal dystrophy syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Infantile onset spinocerebellar ataxia Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Richards-Rundle syndrome Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 3
Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 3
Spinocerebellar ataxia type 7 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 1 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 2 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 6 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 8 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 10 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 4 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 28 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 29 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 31 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 15/16 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 40 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 38 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia with axonal neuropathy type 1 Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
Azorean disease, type I Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Azorean disease, type II Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Azorean disease, type III Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Azorean disease, type IV Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1
X-linked progressive cerebellar ataxia Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
X-linked non progressive cerebellar ataxia Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 2
Contusion of cerebellum due to birth trauma Finding site True Cerebellar structure Inferred relationship Existential restriction modifier 1

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