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DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name ▼ | UniProt ID |
|---|---|---|---|---|---|
| C0023895 | Liver diseases | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0342784 | Pearson's marrow-pancreas syndrome | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C2750441 | LIVER DISEASE, ALCOHOLIC, SUSCEPTIBILITY TO, 1 | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0004245 | Atrioventricular Block | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0016522 | Foramen Ovale, Patent | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C1969443 | Trifunctional Protein Deficiency With Myopathy And Neuropathy | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0026848 | Myopathy | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C3150275 | COMPLEMENT COMPONENT 2 DEFICIENCY | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0020598 | Hypocalcemia | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0282160 | Aplasia Cutis Congenita | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C2711227 | Steatohepatitis | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0206667 | Adrenal Cortical Adenoma | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0524620 | Metabolic Syndrome X | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0007193 | Cardiomyopathy, Dilated | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C3150651 | FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2 | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C2750440 | FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1 | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C3875321 | Inflammatory dermatosis | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0220994 | Hyperammonemia | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0235991 | Small for gestational age (disorder) | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0221757 | alpha 1-Antitrypsin Deficiency | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0032285 | Pneumonia | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0241005 | Creatine phosphokinase serum increased | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0020639 | Hypoproteinemia | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0035410 | Rhabdomyolysis | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0002395 | Alzheimer's Disease | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
