Term Name:	hereditary spastic paraplegia 6
Synonyms:	autosomal dominant familial spastic paraplegia type 3, autosomal dominant spastic paraplegia 6, autosomal dominant spastic paraplegia type 6, FSP3, SPG6
Definition:	A hereditary spastic paraplegia that is usually characterized by rapidly progressive and severe spastic paraplegia and has_material_basis_in mutation in the NIPA1 gene on chromosome 15q11.2.
Ontology:	Human Disease [DOID:0110811]   ( DOID:0110811 )