Pub. Date : 2021 Jan-Dec
PMID : 34284652
1 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Fabry disease (FD) is a progressive, X-linked inherited disorder of glycosphingolipid metabolism due to deficient or absent lysosomal alpha-galactosidase A (alpha-Gal A) activity which results in progressive accumulation of globotriaosylceramide (Gb3) and related metabolites. | globotriaosylceramide | alpha 1,4-galactosyltransferase (P blood group) | Homo sapiens |