Term Name:	hereditary spastic paraplegia 48
Synonyms:	autosomal recessive spastic paraplegia 48, autosomal recessive spastic paraplegia type 48, SPG48
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the AP5Z1 gene on chromosome 7p22.1.
Ontology:	Human Disease [DOID:0110800]   ( DOID:0110800 )