Gaucher disease (GD) is a lysosomal storage disorder encompassing three main forms (types 1, 2 and 3), a fetal form and a variant with cardiac involvement (Gaucher disease - ophthalmoplegia - cardiovascular calcification or Gaucher-like disease). The disease is Gaucher disease (MONDO_0018150, a Monarch Disease Ontology identifier). Also known as: Gaucher syndrome, Gaucher's disease, acid beta-glucosidase deficiency, glocucerebrosidase deficiency, glucocerebrosidase deficiency, glucocerebrosidosis, glucosylceramidase deficiency, glucosylceramide beta-glucosidase deficiency.