Term Name:	hereditary spastic paraplegia 92
Synonyms:	autosomal recessive spastic paraplegia 92, SPG92
Definition:	A hereditary spastic paraplegia that has_material_basis_in homozygous or compound heterozygous mutation in the FICD gene on chromosome 12q23.
Ontology:	Human Disease [DOID:0070644]   ( DOID:0070644 )