Spinocerebellar Ataxia 32 (SCA32)

Alias:

Sca32

Cerebellar Ataxia with Azoospermia and Intellectual Disability

Spinocerebellar Ataxia Type 32

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Spinocerebellar Ataxia 32, also known as sca32, is related to spinocerebellar ataxia, autosomal recessive 32, and has symptoms including cerebellar ataxia Affiliated tissues include brain, and related phenotypes are cognitive impairment and azoospermia

Related ID：

MALACARDS：SPN259

OMIM：613909