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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 |
|---|---|---|---|---|---|
| C0004364 | Autoimmune Diseases | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0023283 | Leishmaniasis, Cutaneous | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0010674 | Cystic Fibrosis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0009319 | Colitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0003850 | Arteriosclerosis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C4282128 | PATENT DUCTUS ARTERIOSUS 1 | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0030409 | Paracoccidioidomycosis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C3714636 | Pneumonitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0243026 | Sepsis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0010414 | Infection by Cryptococcus neoformans | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0019163 | Hepatitis B | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0006845 | Candidiasis, Chronic Mucocutaneous | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C1859353 | Candidiasis, Familial, 2 | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C1306459 | Primary malignant neoplasm | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0085253 | Adult-Onset Still Disease | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0038034 | Sporotrichosis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0024141 | Lupus Erythematosus, Systemic | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C1868684 | EAR, PATELLA, SHORT STATURE SYNDROME | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0006826 | Malignant Neoplasms | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0002395 | Alzheimer's Disease | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0042384 | Vasculitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0028754 | Obesity | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0004943 | Behcet Syndrome | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0026691 | Mucocutaneous Lymph Node Syndrome | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0008582 | Chromoblastomycosis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
