Term Name:	hereditary spastic paraplegia 35
Synonyms:	autosomal recessive spastic paraplegia 35, autosomal recessive spastic paraplegia type 35, FAHN, fatty acid hydroxylase-associated neurodegeneration, leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia, SPG35
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the FA2H gene on chromosome 16q23.1.
Ontology:	Human Disease [DOID:0110786]   ( DOID:0110786 )