Human genes for hereditary spastic paraplegia 3A
Hereditary spastic paraplegia 3A [DOID:0110791]
A hereditary spastic paraplegia that is characterized by lower limb weakness and spasticity that is generally non-progressive or extremely slow and has_material_basis_in mutation in the ATL1 gene on chromosome 14q22.
Synonyms: hereditary spastic paraplegia 3A, DOID:0110791, familial spastic paraplegia 3A, autosomal dominant familial spastic paraplegia 1, autosomal dominant spastic paraplegia 3 ...