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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 ▲ |
|---|---|---|---|---|---|
| C0376358 | Malignant neoplasm of prostate | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0270853 | Juvenile Myoclonic Epilepsy | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0018802 | Congestive heart failure | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0002395 | Alzheimer's Disease | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0008370 | Cholestasis | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0011615 | Dermatitis, Atopic | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0036572 | Seizures | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0013595 | Eczema | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0001973 | Alcoholic Intoxication, Chronic | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0010346 | Crohn Disease | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C1839839 | MAJOR AFFECTIVE DISORDER 2 | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0018784 | Sensorineural Hearing Loss (disorder) | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C3536893 | Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0019158 | Hepatitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0006840 | Candidiasis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0018889 | Helminthiasis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0024117 | Chronic Obstructive Airway Disease | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0700345 | Candidiasis, Vulvovaginal | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C1394891 | Intrinsic Factor Deficiency | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0022568 | Keratitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0026946 | Mycoses | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0041296 | Tuberculosis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C1262117 | Fungal keratitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0037299 | Skin Ulcer | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0345904 | Malignant neoplasm of liver | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
