Fabry Disease


Anderson Fabry Disease

Anderson-Fabry Disease

Angiokeratoma Corporis Diffusum

Angiokeratoma Diffuse

Angiokeratoma, Diffuse

Ceramide Trihexosidase Deficiency

Deficiency, Ceramide Trihexosidase

Deficiency, GLA

Deficiency, alpha-Galactosidase A

Diffuse Angiokeratoma

Fabry's Disease

GLA Deficiency

Hereditary Dystopic Lipidosis

Lipidosis, Hereditary Dystopic

alpha Galactosidase A Deficiency

alpha Galactosidase A Deficiency Disease

alpha-Galactosidase A Deficiency

alpha-Galactosidase A Deficiency Disease

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.