Term Name:	hereditary spastic paraplegia 63
Synonyms:	autosomal recessive spastic paraplegia 63, spastic paraplegia 63, SPG63
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the AMPD2 gene on chromosome 1p13.
Ontology:	Human Disease [DOID:0110814]   ( DOID:0110814 )