Term Name:	hereditary spastic paraplegia 73
Synonyms:	autosomal dominant spastic paraplegia 73, autosomal dominant spastic paraplegia type 73, SPG73
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the CPT1C gene on chromosome 19q13.
Ontology:	Human Disease [DOID:0110818]   ( DOID:0110818 )