hereditary spastic paraplegia 31 (DOID:0110782)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 31; autosomal dominant spastic paraplegia type 31; SPG31
Alt IDs: OMIM:610250, ICD10CM:G11.4, ORDO:101011
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP1 gene on chromosome 2p11.