Term Name:	hereditary spastic paraplegia 32
Synonyms:	autosomal recessive spastic paraplegia 32, autosomal recessive spastic paraplegia type 32, SPG32
Definition:	A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 14q12-q21.
Ontology:	Human Disease [DOID:0110783]   ( DOID:0110783 )