hereditary spastic paraplegia 89 (DOID:0070458)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 89; SPG89
Alt IDs: OMIM:620379
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.