DISEASES

Disease-gene associations mined from literature

Human genes for dentatorubral-pallidoluysian atrophy

Dentatorubral-pallidoluysian atrophy [DOID:0060162]

A spinocerebellar degeneration that has_material_basis_in an expansion of a CAG repeat encoding a polyglutamine tract in the atrophin-1 protein.

Synonyms:  dentatorubral-pallidoluysian atrophy,  DOID:0060162,  dentatorubralpallidoluysian atrophy,  DRPLA,  Haw River Syndrome ...

Linkouts:  OMIM