Fabry Disease (Fabry's Disease)
870
relevant articles (24 outcomes,
79 trials/studies)
found for this Disease
Description:
An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other GLYCOSPHINGOLIPIDS in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders.
Also Known As:
Fabry's Disease; Anderson Fabry Disease; Disease, Fabry; Angiokeratoma Corporis Diffusum; alpha-Galactosidase A Deficiency Disease; Fabrys Disease; alpha Galactosidase A Deficiency Disease; Anderson-Fabry Disease
Relationship Network
Disease Context: Research Results