Term Name:	hereditary spastic paraplegia 5A
Synonyms:	autosomal recessive spastic paraplegia 5A, autosomal recessive spastic paraplegia type 5A, SPG5A
Definition:	A hereditary spastic paraplegia that is characterized by progressive muscle weakness and paraplegia and has_material_basis_in mutation in the CYP7B1 gene on chromosome 8q12.
Ontology:	Human Disease [DOID:0110810]   ( DOID:0110810 )