Term Name:	hereditary spastic paraplegia 36
Synonyms:	autosomal dominant spastic paraplegia 36, autosomal dominant spastic paraplegia type 36, SPG36
Definition:	A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 12q23-q24.
Ontology:	Human Disease [DOID:0110787]   ( DOID:0110787 )