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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 ▼ |
|---|---|---|---|---|---|
| C0014457 | Eosinophilia | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
| C0282687 | Hemorrhagic Fever, Ebola | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
| C0010346 | Crohn Disease | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
| C0042769 | Virus Diseases | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
| C0024117 | Chronic Obstructive Airway Disease | GALNT13 | 114805 | polypeptide N-acetylgalactosaminyltransferase 13 | Q8IUC8 |
| C0242379 | Malignant neoplasm of lung | GALNT13 | 114805 | polypeptide N-acetylgalactosaminyltransferase 13 | Q8IUC8 |
| C0002895 | Anemia, Sickle Cell | GALNT13 | 114805 | polypeptide N-acetylgalactosaminyltransferase 13 | Q8IUC8 |
| C0027651 | Neoplasms | GALNT13 | 114805 | polypeptide N-acetylgalactosaminyltransferase 13 | Q8IUC8 |
| C3554349 | ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 9 | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C0079154 | Congenital Nonbullous Ichthyosiform Erythroderma | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C0020758 | Congenital ichthyosis | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C0013336 | Dwarfism | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C1384666 | hearing impairment | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C4551675 | Keratoderma, Palmoplantar | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C0020620 | Hypohidrosis | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C0013592 | Ectropion | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C0011615 | Dermatitis, Atopic | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C0020757 | Ichthyoses | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C0079583 | Ichthyosiform Erythroderma, Congenital | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C0013595 | Eczema | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C0011603 | Dermatitis | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C0002170 | Alopecia | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C2750787 | Weill-Marchesani-Like Syndrome | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C0022568 | Keratitis | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C0006826 | Malignant Neoplasms | KLB | 152831 | klotho beta | Q86Z14 |
