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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 |
|---|---|---|---|---|---|
| C0042109 | Urticaria | ELOVL4 | 6785 | ELOVL fatty acid elongase 4 | Q9GZR5 |
| 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 |
| C2239176 | Liver carcinoma | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C4539754 | ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 14 | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C0476089 | Endometrial Carcinoma | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C0013336 | Dwarfism | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C0870082 | Hyperkeratosis | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C0008370 | Cholestasis | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C4551630 | Ichthyosis Congenita I | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C0376358 | Malignant neoplasm of prostate | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C3888093 | ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2 | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C0013592 | Ectropion | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C0079583 | Ichthyosiform Erythroderma, Congenital | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C0153452 | Malignant neoplasm of gallbladder | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C0235782 | Gallbladder Carcinoma | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C0271441 | Chronic otitis media | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
