Pub. Date : 2012 Dec
PMID : 23007467
4 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Fabry disease is a lysosomal storage disorder (LSD) caused by deficiency of alpha-galactosidase A (alpha-gal A), resulting in deposition of globotriaosylceramide (Gb3; also known as ceramide trihexoside) in the vascular endothelium of many organs. | globotriaosylceramide | galactosidase, alpha | Mus musculus |
| 2 | Fabry disease is a lysosomal storage disorder (LSD) caused by deficiency of alpha-galactosidase A (alpha-gal A), resulting in deposition of globotriaosylceramide (Gb3; also known as ceramide trihexoside) in the vascular endothelium of many organs. | globotriaosylceramide | galactosidase, alpha | Mus musculus |
| 3 | Fabry disease is a lysosomal storage disorder (LSD) caused by deficiency of alpha-galactosidase A (alpha-gal A), resulting in deposition of globotriaosylceramide (Gb3; also known as ceramide trihexoside) in the vascular endothelium of many organs. | globotriaosylceramide | galactosidase, alpha | Mus musculus |
| 4 | Fabry disease is a lysosomal storage disorder (LSD) caused by deficiency of alpha-galactosidase A (alpha-gal A), resulting in deposition of globotriaosylceramide (Gb3; also known as ceramide trihexoside) in the vascular endothelium of many organs. | globotriaosylceramide | galactosidase, alpha | Mus musculus |