Human genes for spastic ataxia 1
Spastic ataxia 1 [DOID:0050772]
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.
Synonyms: spastic ataxia 1, DOID:0050772