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Autosomal dominant cerebellar ataxia type I

rare

Autosomal dominant cerebellar ataxia (ADCA) type I is a group of spinocerebellar ataxias (SCAs) characterized by ataxia with other neurological signs, including oculomotor disturbances, cognitive deficits, pyramidal and extrapyramidal dysfunction, bulbar, spinal and peripheral nervous system involvement.

Identifiers
MONDO:0019792 Orphanet:94145
Part of
Autosomal dominant cerebellar ataxia
Also known as
ADCA1 · ADCAI · autosomal dominant cerebellar ataxia type 1 · cerebellar plus syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Machado-Joseph disease 4
Spinocerebellar ataxia type 2 1
Autosomal dominant cerebellar ataxia, deafness and narcolepsy
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome
Cerebellar dysfunction with variable cognitive and behavioral abnormalities
Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism
Spinocerebellar ataxia 46
Spinocerebellar ataxia type 1
Spinocerebellar ataxia type 12
Spinocerebellar ataxia type 13
Spinocerebellar ataxia type 14
Spinocerebellar ataxia type 15/16
Spinocerebellar ataxia type 17
Spinocerebellar ataxia type 18
Spinocerebellar ataxia type 19/22
Spinocerebellar ataxia type 20
Spinocerebellar ataxia type 21
Spinocerebellar ataxia type 23
Spinocerebellar ataxia type 25
Spinocerebellar ataxia type 27
Spinocerebellar ataxia type 28
Spinocerebellar ataxia type 29
Spinocerebellar ataxia type 32
Spinocerebellar ataxia type 34
Spinocerebellar ataxia type 35
Spinocerebellar ataxia type 36
Spinocerebellar ataxia type 37
Spinocerebellar ataxia type 4
Spinocerebellar ataxia type 40
Spinocerebellar ataxia type 8

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