Fabry disease (FD) is a progressive, inherited, multisystemic lysosomal storage disease characterized by specific neurological, cutaneous, renal, cardiovascular, cochleo-vestibular and cerebrovascular manifestations. The disease is Fabry disease (Monarch Disease Ontology id MONDO_0010526). Also known as: Alpha-galactosidase A deficiency, Anderson-Fabry disease, FD, Fabry's disease, Fd, alpha galactosidase deficiency, angiokeratoma corporis diffusum, deficiency of melibiase.