Catalog
Autosomal dominant cerebellar ataxia type 1
No MMS code
Link to WHO Definition
Autosomal dominant cerebellar ataxia type 1 – http://id.who.int/icd/entity/1919353698
Type I autosomal dominant cerebellar ataxia (ADCA) is a group of spinocerebellar ataxias (SCA) characterised by ataxia with other neurological signs, including oculomotor disturbances, cognitive deficits, pyramidal and extrapyramidal dysfunction, bulbar, spinal and peripheral nervous system involvement.
Parents
Children
- Spinocerebellar ataxia type 17
- Spinocerebellar ataxia type 13
- Spinocerebellar ataxia type 12
- Spinocerebellar ataxia type 2
- Spinocerebellar ataxia type 23
- Spinocerebellar ataxia type 32
- Spinocerebellar ataxia type 27
- Spinocerebellar ataxia type 21
- Spinocerebellar ataxia type 36
- Spinocerebellar ataxia type 18
- Spinocerebellar ataxia type 35
- Spinocerebellar ataxia type 4
- Spinocerebellar ataxia type 8
- Spinocerebellar ataxia type 19
- Spinocerebellar ataxia type 22
- Spinocerebellar ataxia type 3
- Spinocerebellar ataxia type 28
- Spinocerebellar ataxia type 1
- Spinocerebellar ataxia type 16