Term Name:	hereditary spastic paraplegia 26
Synonyms:	autosomal recessive spastic paraplegia 26, autosomal recessive spastic paraplegia type 26, GM2 synthase deficiency, SPG26
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the B4GALNT1 gene on chromosome 12q13.
Ontology:	Human Disease [DOID:0110777]   ( DOID:0110777 )