Term Name:	hereditary spastic paraplegia 76
Synonyms:	autosomal recessive spastic paraplegia 76, SPG76
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the CAPN1 gene on chromosome 11q13.
Ontology:	Human Disease [DOID:0110821]   ( DOID:0110821 )