230232005: Late onset cerebellar ataxia (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding related to coordination / incoordination (finding)\Ataxia\Late onset cerebellar ataxia

\Disease\Late onset cerebellar ataxia

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

Descriptions:

Id Description Lang Type Status Case? Module

345043010 Late onset cerebellar ataxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

618014015 Late onset cerebellar ataxia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5931911000241112 ataxie cérébelleuse à début tardif fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Late onset cerebellar ataxia	Is a	Cerebellar ataxia	false	Inferred relationship	Some
Late onset cerebellar ataxia	Finding site	Cerebellar structure	false	Inferred relationship	Some	1
Late onset cerebellar ataxia	Associated morphology	dégénérescence	false	Inferred relationship	Some	1
Late onset cerebellar ataxia	Associated morphology	dégénérescence	false	Inferred relationship	Some	1
Late onset cerebellar ataxia	Finding site	Cerebellar structure	false	Inferred relationship	Some
Late onset cerebellar ataxia	Is a	Ataxia	true	Inferred relationship	Some
Late onset cerebellar ataxia	Is a	Disease	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Progressive cerebellar ataxia	Is a	True	Late onset cerebellar ataxia	Inferred relationship	Some
Periodic ataxia	Is a	True	Late onset cerebellar ataxia	Inferred relationship	Some
Progressive spinocerebellar ataxia with decreased tendon reflexes	Is a	True	Late onset cerebellar ataxia	Inferred relationship	Some
Progressive spinocerebellar ataxia with retained tendon reflexes	Is a	True	Late onset cerebellar ataxia	Inferred relationship	Some
Progressive cerebellar ataxia with palatal myoclonus	Is a	True	Late onset cerebellar ataxia	Inferred relationship	Some
Progressive cerebellar ataxia with hypogonadism	Is a	False	Late onset cerebellar ataxia	Inferred relationship	Some
Olivopontocerebellar degeneration	Is a	True	Late onset cerebellar ataxia	Inferred relationship	Some
Azorean disease	Is a	True	Late onset cerebellar ataxia	Inferred relationship	Some
A rare disorder characterized by a slowly progressive pure cerebellar ataxia associated with dysarthria. It has been described in 53 individuals from 26 families of Canadian origin. The mode of transmission is autosomal recessive. Positional cloning has led to the identification of several gene mutations.	Is a	True	Late onset cerebellar ataxia	Inferred relationship	Some
A rare non-hereditary degenerative ataxia disease characterized by a slowly progressive cerebellar syndrome (with ataxia of stance and gait, upper limb dysmetria and intention tremor, ataxic speech, and oculomotor abnormalities), presenting in adulthood (at around 50 years of age), that is not due to a known cause. Extracerebellar symptoms (e.g., decreased vibration sense and absent or decreased ankle reflexes), polyneuropathy and mild autonomic dysfunction may also be present. Mild cognitive impairment has also rarely been reported.	Is a	True	Late onset cerebellar ataxia	Inferred relationship	Some
A rare, hereditary, cerebellar ataxia disorder characterized by late-onset spinocerebellar ataxia, manifesting with slowly progressive gait disturbances, dysarthria, limb and truncal ataxia, and smooth-pursuit eye movement disturbance, associated with a history of psychomotor delay from childhood. Mild atrophy of the cerebellar vermis and hemispheres is observed on brain imaging.	Is a	True	Late onset cerebellar ataxia	Inferred relationship	Some

This concept is not in any reference sets