DISEASES

Disease-gene associations mined from literature

Human genes for infantile onset spinocerebellar ataxia

Infantile onset spinocerebellar ataxia [DOID:0050556]

Spinocerebellar ataxia (SCA) is a progressive, degenerative, genetic disease with multiple types, each of which could be considered a disease in its own right.

Synonyms:  infantile onset spinocerebellar ataxia,  DOID:0050556,  OHAHA SYNDROME,  OHAHA disease,  OHAHA disorder

Linkouts:  OMIM