Human genes for hereditary spastic paraplegia 13
Hereditary spastic paraplegia 13 [DOID:0110766]
A hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has_material_basis_in mutation in the HSPD1 on chromosome 2q33.
Synonyms: hereditary spastic paraplegia 13, DOID:0110766, familial spastic paraplegia 13, autosomal dominant spastic paraplegia 13, SPG13