BioScience Dictionary

 
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Found Fabry disease 1 time.

Displaying results 1 to 10.

1. Fabry disease
An X-linked genetic disease in which the gene coding for the enzyme alpha-galactosidase A (a type of galactosidase ) is nonfunctional. As a result, sphingolipid and glycolipid compounds accumulate in the blood vessel walls of people with the disease, eventually causing vascular malfunctions.