Term Name:	hereditary spastic paraplegia 9B
Synonyms:	autosomal recessive complex spastic paraplegia type 9B, autosomal recessive spastic paraplegia 9B, SPG9B
Definition:	A hereditary spastic paraplegia that has_material_basis_in autosomal recessive homozygous or compound heterozygous mutation in the ALDH18A1 gene on chromosome 10q24.
Ontology:	Human Disease [DOID:0110825]   ( DOID:0110825 )