hereditary spastic paraplegia 56 (DOID:0110808)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 56; autosomal recessive spastic paraplegia type 56; SPG56
Alt IDs: OMIM:615030, ICD10CM:G11.4, ORDO:320411
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the CYP2U1 gene on chromosome 4q25.