hereditary spastic paraplegia 13 (DOID:0110766)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 13; SPG13
Alt IDs: OMIM:605280, ICD10CM:G11.4, ORDO:100994
Definition: 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 gene on chromosome 2q33.