Term Name:	hereditary spastic paraplegia 43
Synonyms:	autosomal recessive spastic paraplegia 43, autosomal recessive spastic paraplegia type 43, SPG43
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the C19ORF12 gene on chromosome 19q12.
Ontology:	Human Disease [DOID:0110795]   ( DOID:0110795 )