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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 |
|---|---|---|---|---|---|
| C0015469 | Facial paralysis | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
| C0022661 | Kidney Failure, Chronic | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
| C0036572 | Seizures | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
| C2239176 | Liver carcinoma | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
| C0036341 | Schizophrenia | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
| C0014544 | Epilepsy | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
| C0006826 | Malignant Neoplasms | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
| C0036439 | Scoliosis, unspecified | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
| C1956346 | Coronary Artery Disease | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
| C0878544 | Cardiomyopathies | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
| C0033975 | Psychotic Disorders | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
| C1561643 | Chronic Kidney Diseases | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
| C1959583 | Myocardial Failure | ACADS | 35 | acyl-CoA dehydrogenase short chain | P16219 |
| C0018801 | Heart failure | ACADM | 34 | acyl-CoA dehydrogenase medium chain | P11310 |
| C0220710 | Medium-chain acyl-coenzyme A dehydrogenase deficiency | ACADM | 34 | acyl-CoA dehydrogenase medium chain | P11310 |
| C0038644 | Sudden infant death syndrome | ACADM | 34 | acyl-CoA dehydrogenase medium chain | P11310 |
| C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | ACADM | 34 | acyl-CoA dehydrogenase medium chain | P11310 |
| C0020617 | Hypoglycemic coma | ACADM | 34 | acyl-CoA dehydrogenase medium chain | P11310 |
| C0031485 | Phenylketonurias | ACADM | 34 | acyl-CoA dehydrogenase medium chain | P11310 |
| C0342788 | Renal carnitine transport defect | ACADM | 34 | acyl-CoA dehydrogenase medium chain | P11310 |
| C0025521 | Inborn Errors of Metabolism | ACADM | 34 | acyl-CoA dehydrogenase medium chain | P11310 |
| C0003872 | Arthritis, Psoriatic | ACADM | 34 | acyl-CoA dehydrogenase medium chain | P11310 |
| C0524851 | Neurodegenerative Disorders | ACADM | 34 | acyl-CoA dehydrogenase medium chain | P11310 |
| C0023895 | Liver diseases | ACADM | 34 | acyl-CoA dehydrogenase medium chain | P11310 |
| C0006114 | Cerebral Edema | ACADM | 34 | acyl-CoA dehydrogenase medium chain | P11310 |
