spastic ataxia 1 (DOID:0050772)
Alliance: disease page
Alt IDs: OMIM:108600
Definition: A spastic ataxia characterized by early-onset cerebellar ataxia, spasticity, pyramidal syndrome and peripheral neuropathy, has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the VAMP1 gene on chromosome 12p13.