hereditary spastic paraplegia 9B (DOID:0110825)
Alliance: disease page
Synonyms: autosomal recessive complex spastic paraplegia type 9B; autosomal recessive spastic paraplegia 9B; SPG9B
Alt IDs: OMIM:616586, ICD10CM:G11.4, ORDO:447760
Definition: A hereditary spastic paraplegia that has_material_basis_in autosomal recessive homozygous or compound heterozygous mutation in the ALDH18A1 gene on chromosome 10q24.