Autosomal dominant cerebellar ataxia type I

MONDO:0019792

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.

Also known as: ADCA1, ADCAI, autosomal dominant cerebellar ataxia type 1, cerebellar plus syndrome

35 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant cerebellar ataxia type I itself.

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↑ Autosomal dominant cerebellar ataxia (33)

Sub-types of Autosomal dominant cerebellar ataxia type I

Machado-Joseph disease 11 trials
4 sub-types
- Machado-Joseph disease type 3 2 trials
- Machado-Joseph disease type 1 0 trials
- Machado-Joseph disease type 2 0 trials
- Machado-Joseph disease type 4 0 trials
Spinocerebellar ataxia type 1 10 trials
Spinocerebellar ataxia type 2 10 trials
1 sub-type
- Spinocerebellar degeneration with slow eye movements 0 trials
Spinocerebellar ataxia type 8 4 trials
Spinocerebellar ataxia type 27 2 trials
Spinocerebellar ataxia type 23 1 trial
Spinocerebellar ataxia type 29 1 trial
Autosomal dominant cerebellar ataxia, deafness and narcolepsy 0 trials
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome 0 trials
Cerebellar dysfunction with variable cognitive and behavioral abnormalities 0 trials
Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism 0 trials
Spinocerebellar ataxia 46 0 trials
Spinocerebellar ataxia type 12 0 trials
Spinocerebellar ataxia type 13 0 trials
Spinocerebellar ataxia type 14 0 trials
Spinocerebellar ataxia type 15/16 0 trials
Spinocerebellar ataxia type 17 0 trials
Spinocerebellar ataxia type 18 0 trials
Spinocerebellar ataxia type 19/22 0 trials
Spinocerebellar ataxia type 20 0 trials
Spinocerebellar ataxia type 21 0 trials
Spinocerebellar ataxia type 25 0 trials
Spinocerebellar ataxia type 28 0 trials
Spinocerebellar ataxia type 32 0 trials
Spinocerebellar ataxia type 34 0 trials
Spinocerebellar ataxia type 35 0 trials
Spinocerebellar ataxia type 36 0 trials
Spinocerebellar ataxia type 37 0 trials
Spinocerebellar ataxia type 4 0 trials
Spinocerebellar ataxia type 40 0 trials

Including sub-types (35) Tagged with Autosomal dominant cerebellar ataxia type I (0)

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