Other terms
Disease, Fabry,Fabry's Disease,Fabrys Disease,Angiokeratoma Corporis Diffusum,alpha-Galactosidase A Deficiency Disease,alpha Galactosidase A Deficiency Disease,Anderson-Fabry Disease,Anderson Fabry Disease,alpha-Galactosidase A Deficiency,Deficiencies, alpha-Galactosidase A,Deficiency, alpha-Galactosidase A,alpha Galactosidase A Deficiency,alpha-Galactosidase A Deficiencies
Description
Fabry 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.
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