Term Name:	hereditary spastic paraplegia 81
Synonyms:	autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction, autosomal recessive complex SPG due to Kennedy pathway dysfunction, spastic paraplegia 81 autosomal recessive, SPG81
Definition:	A hereditary spastic paraplegia characterized by onset in infancy, delayed motor development, progressive spasticity, and other neurologic impairments that has_material_basis_in homozygous or compound heterozygous mutation in the SELENOI gene on chromosome 2p23.3.
Ontology:	Human Disease [DOID:0112349]   ( DOID:0112349 )