- ceramide trihexosidase
- cer·a·mide tri·hex·o·si·dase (serґə-mīd tri″hek-soґsĭ-dās) α-galactosidase A.
Medical dictionary. 2011.
ceramide trihexosidase
Look at other dictionaries:
ceramide trihexosidase deficiency — cer·a·mide tri·hex·o·si·dase de·fi·cien·cy (serґə mīd tri″hek soґsĭ dās) Fabry disease … Medical dictionary
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Fabry disease — A genetic disease due to deficiency of an enzyme called alpha galactosidase A. This enzyme is essential to the metabolism of molecules known as glycosphingolipids. Without the enzyme, glycosphingolipids accumulate in the kidneys, heart, nerves… … Medical dictionary
Fabry disease — (= angiokeratoma) Storage disease due to deficiency of ceramide trihexosidase … Dictionary of molecular biology
