Term Name:	hereditary spastic paraplegia 42
Synonyms:	autosomal dominant spastic paraplegia 42, autosomal dominant spastic paraplegia type 42, SPG42
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the SLC33A1 gene on chromosome 3q25.31.
Ontology:	Human Disease [DOID:0110794]   ( DOID:0110794 )