Term Name:	hereditary spastic paraplegia 53
Synonyms:	autosomal recessive spastic paraplegia 53, autosomal recessive spastic paraplegia type 53, SPG53
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the VPS37A gene on chromosome 8p22.
Ontology:	Human Disease [DOID:0110805]   (DOID:0110805)