Fabry Disease |
|
| Fabry's Disease; Anderson Fabry Disease; Disease, Anderson-Fabry; Disease, Fabry; Disease, Fabry's; Fabrys Disease | |
| Lysosomal storage disease caused by a deficiency of alpha-galactosidase A and resulting in an accumulation of globotriaosylceramide in the renal and cardiovascular systems. The disease is X-linked and is characterized by telangiectatic skin lesions, renal failure, and disturbances of the cardiovascular, gastrointestinal, and central nervous systems. | |