hereditary spastic paraplegia 48 (DOID:0110800)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 48; autosomal recessive spastic paraplegia type 48; SPG48
Alt IDs: OMIM:613647, ICD10CM:G11.4, ORDO:306511
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the AP5Z1 gene on chromosome 7p22.1.