Term Name:	hereditary spastic paraplegia 49
Synonyms:	autosomal recessive spastic paraplegia 49, autosomal recessive spastic paraplegia type 49, SPG49
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the TECPR2 gene on chromosome 14q32.
Ontology:	Human Disease [DOID:0110801]   ( DOID:0110801 )