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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 ▼ |
|---|---|---|---|---|---|
| C0020758 | Congenital ichthyosis | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0007758 | Cerebellar Ataxia | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0037268 | Skin Abnormalities | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0087012 | Ataxia, Spinocerebellar | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0023903 | Liver neoplasms | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C1864446 | Retinitis Pigmentosa 25 | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0011847 | Diabetes | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0027651 | Neoplasms | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0339527 | Leber Congenital Amaurosis | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0079583 | Ichthyosiform Erythroderma, Congenital | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| C0004153 | Atherosclerosis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0011849 | Diabetes Mellitus | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0041296 | Tuberculosis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0004238 | Atrial Fibrillation | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0011847 | Diabetes | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0041327 | Tuberculosis, Pulmonary | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0678222 | Breast Carcinoma | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0010346 | Crohn Disease | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0029408 | Degenerative polyarthritis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0236970 | Alcohol-Induced Disorders | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0039585 | Androgen-Insensitivity Syndrome | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0700095 | Central neuroblastoma | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0020179 | Huntington Disease | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C4225234 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0243026 | Sepsis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
