Term Name:	hereditary spastic paraplegia 52
Synonyms:	autosomal recessive spastic paraplegia 52, CPSQ6, spastic quadriplegic cerebral palsy 6, SPG52
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the AP4S1 gene on chromosome 14q12.
Ontology:	Human Disease [DOID:0110804]   ( DOID:0110804 )