Term Name:	hereditary spastic paraplegia 89
Synonyms:	autosomal recessive spastic paraplegia 89, SPG89
Definition:	A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that has_material_basis_in homozygous mutation in the AMFR gene on chromosome 16q13.
Ontology:	Human Disease [DOID:0070458]   ( DOID:0070458 )