Term Name:	hereditary spastic paraplegia 56
Synonyms:	autosomal recessive spastic paraplegia 56, autosomal recessive spastic paraplegia type 56, SPG56
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the CYP2U1 gene on chromosome 4q25.
Ontology:	Human Disease [DOID:0110808]   ( DOID:0110808 )