Fabry disease, also known as Anderson–Fabry disease, is a rare genetic disease that can affect many parts of the body, including the kidneys, heart, brain, and skin. [1]

Fabry disease is a rare genetic lysosomal storage disorder, where you don’t have enough of a certain enzyme that breaks down fats. These fats collect in blood vessels and tissues, raising …

Fabry disease is an inherited disorder that results from the buildup of a type of fat, called globotriaosylceramide, in the body's cells. Beginning in childhood, this buildup causes signs …

Oct 14, 2024 · Learn more about Fabry disease, including its symptoms, what causes it, and how it's treated.

Milder forms of Fabry disease may appear later in life and affect only the heart or kidneys. Fabry disease is caused by certain changes (pathogenic variants, also called genetic changes) in the …

What Is Fabry Disease? Fabry disease is a rare genetic disorder caused by a defective gene (the GLA gene) in the body. In most cases, the defect in the gene causes a deficient quantity of the …

Aug 7, 2025 · What is Fabry Disease? Fabry disease is a rare disorder that happens when the body lacks an important enzyme called alpha-galactosidase A (alpha GAL). This enzyme …

Sep 11, 2025 · Fabry disease is a rare genetic disorder that can affect many organs, resulting in a wide range of symptoms. Learn its symptoms, causes, treatment, and more.

Fabry disease is a disorder of glycosphingolipid metabolism caused by the functional deficiency of the lysosomal alpha-galactosidase due to pathogenic variants in the GLA gene (Xq21.3-q22).

Jul 4, 2025 · Are you a health care provider looking for information on Fabry disease? Get a brief, comprehensive overview here.