Term Name: nonprogressive cerebellar ataxia with mental retardation
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by early onset of nonprogressive cerebellar ataxia, developmental delay, intellectual impairment and cerebellar atrophy, and has_material_basis_in autosomal dominant inheritance of mutation in the CAMTA1 gene.
Ontology: Human Disease [DOID:0050998]   ( DOID:0050998 )

Relationships
is a type of: autosomal dominant cerebellar ataxia