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 )

Relationships
is a type of: autosomal recessive disease hereditary spastic paraplegia