What is another word for Anderson Fabry Disease?
Pronunciation: [ˈandəsən fˈabɹi dɪzˈiːz] (IPA) 
Anderson Fabry Disease, also known as Fabry disease, is a rare genetic disorder that affects multiple organs in the body. It is caused by the mutation of a gene responsible for producing an enzyme called alpha-galactosidase A. This enzyme deficiency leads to the accumulation of a specific type of fat, known as globotriaosylceramide, in various tissues and organs. Other names for Anderson Fabry Disease include Fabry syndrome, Fabry's disease, and Fabry's syndrome. While the disease is relatively uncommon, it is important to raise awareness about it due to its debilitating effects on individuals and the need for early diagnosis and management.
