Term Name:	galactosialidosis
Synonyms:
Definition:	A lysosomal storage disease that is characterized by combined deficiency of beta-galactosidase and neuraminidase that has_material_basis_in homozygous or compound heterozygous mutation in the CTSA gene on chromosome 20q13.
Ontology:	Human Disease [DOID:0080540]   ( DOID:0080540 )