Term Name:	hereditary spastic paraplegia 51
Synonyms:	autosomal dominant spastic paraplegia 51, CPSQ4, spastic quadriplegic cerebral palsy 4, SPG51
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the AP4E1 gene on chromosome 15q21.
Ontology:	Human Disease [DOID:0110803]   ( DOID:0110803 )