| BioCyc:HUMAN_PWY-7840 |
gala-series glycosphingolipids biosynthesis |
| BioCyc:META_PWY-7840 |
gala-series glycosphingolipids biosynthesis |
| Reactome:R-HSA-9840309 |
Glycosphingolipid biosynthesis |
| Reactome:R-MMU-9840309 |
Glycosphingolipid biosynthesis |
| Reactome:R-RNO-9840309 |
Glycosphingolipid biosynthesis |
| Reactome:R-MMU-1430728 |
Metabolism |
| Reactome:R-MMU-556833 |
Metabolism of lipids |
| Reactome:R-RNO-1660662 |
Glycosphingolipid metabolism |
| Reactome:R-HSA-556833 |
Metabolism of lipids |
| Reactome:R-HSA-428157 |
Sphingolipid metabolism |
| Reactome:R-MMU-1660662 |
Glycosphingolipid metabolism |
| Reactome:R-HSA-1660662 |
Glycosphingolipid metabolism |
| Reactome:R-MMU-428157 |
Sphingolipid metabolism |
| Reactome:R-RNO-1430728 |
Metabolism |
| Reactome:R-RNO-556833 |
Metabolism of lipids |
| Reactome:R-HSA-1430728 |
Metabolism |
| Reactome:R-RNO-428157 |
Sphingolipid metabolism |
| WikiPathways:WP5275 |
Ether lipid biosynthesis |
| WikiPathways:WP4142 |
Metabolism of sphingolipids in ER and Golgi apparatus |
| PathBank:SMP0120702 |
Globoid Cell Leukodystrophy |
| PathBank:SMP0120738 |
Metachromatic Leukodystrophy (MLD) |
| PathBank:SMP0120810 |
Krabbe Disease |
| PathBank:SMP0120492 |
Hereditary Coproporphyria (HCP) |
| PathBank:SMP0120544 |
Porphyria Variegata (PV) |
| PathBank:SMP0120617 |
Glycogenosis, Type III. Cori Disease, Debrancher Glycogenosis |
| PathBank:SMP0120621 |
Sucrase-Isomaltase Deficiency |
| PathBank:SMP0120629 |
Aromatase Deficiency |
| PathBank:SMP0000349 |
Gaucher Disease |
| PathBank:SMP0063673 |
Starch and Sucrose Metabolism |
| PathBank:SMP0120701 |
Gaucher Disease |
| PathBank:SMP0120809 |
Fabry Disease |
| PathBank:SMP0120447 |
Acute Intermittent Porphyria |
| PathBank:SMP0120616 |
Glycogen Synthetase Deficiency |
| PathBank:SMP0120620 |
Mucopolysaccharidosis VII. Sly Syndrome |
| PathBank:SMP0087337 |
Sphingolipid Metabolism |
| PathBank:SMP0063655 |
Porphyrin Metabolism |
| PathBank:SMP0120437 |
17-beta Hydroxysteroid Dehydrogenase III Deficiency |
| PathBank:SMP0120469 |
Congenital Erythropoietic Porphyria (CEP) or Gunther Disease |
| PathBank:SMP0120618 |
Glycogenosis, Type IV. Amylopectinosis, Anderson Disease |
| PathBank:SMP0000348 |
Globoid Cell Leukodystrophy |
| PathBank:SMP0000525 |
Fabry Disease |
| PathBank:SMP0063594 |
Androgen and Estrogen Metabolism |
| PathBank:SMP0120619 |
Glycogenosis, Type VI. Hers Disease |
| PathBank:SMP0000034 |
Sphingolipid Metabolism |
| PathBank:SMP0000347 |
Metachromatic Leukodystrophy (MLD) |
| PathBank:SMP0000526 |
Krabbe Disease |