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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 |
|---|---|---|---|---|---|
| C0155336 | Esotropia with accommodative compensation | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0028754 | Obesity | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0400966 | Non-alcoholic Fatty Liver Disease | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0027051 | Myocardial Infarction | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0006826 | Malignant Neoplasms | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0345904 | Malignant neoplasm of liver | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0235527 | Heart Failure, Right-Sided | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C3875321 | Inflammatory dermatosis | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0751295 | Memory Loss | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0162820 | Dermatitis, Allergic Contact | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0684249 | Carcinoma of lung | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0030567 | Parkinson Disease | ELOVL7 | 79993 | ELOVL fatty acid elongase 7 | A1L3X0 |
| C0162836 | Hidradenitis Suppurativa | ELOVL7 | 79993 | ELOVL fatty acid elongase 7 | A1L3X0 |
| C0027651 | Neoplasms | ELOVL7 | 79993 | ELOVL fatty acid elongase 7 | A1L3X0 |
| C0037019 | Shy-Drager Syndrome | ELOVL7 | 79993 | ELOVL fatty acid elongase 7 | A1L3X0 |
| C0600139 | Prostate carcinoma | ELOVL7 | 79993 | ELOVL fatty acid elongase 7 | A1L3X0 |
| C0376358 | Malignant neoplasm of prostate | ELOVL7 | 79993 | ELOVL fatty acid elongase 7 | A1L3X0 |
| C0021390 | Inflammatory Bowel Diseases | ELOVL7 | 79993 | ELOVL fatty acid elongase 7 | A1L3X0 |
| C0393571 | Multiple System Atrophy | ELOVL7 | 79993 | ELOVL fatty acid elongase 7 | A1L3X0 |
| C0751783 | Lafora Disease | EPM2A | 7957 | EPM2A glucan phosphatase, laforin | O95278 |
| C0751778 | Myoclonic Epilepsies, Progressive | EPM2A | 7957 | EPM2A glucan phosphatase, laforin | O95278 |
| C0206687 | Carcinoma, Endometrioid | EPM2A | 7957 | EPM2A glucan phosphatase, laforin | O95278 |
| C0684276 | Hypsarrhythmia | EPM2A | 7957 | EPM2A glucan phosphatase, laforin | O95278 |
| C0014544 | Epilepsy | EPM2A | 7957 | EPM2A glucan phosphatase, laforin | O95278 |
| C0476254 | Dyslexia | EPM2A | 7957 | EPM2A glucan phosphatase, laforin | O95278 |
