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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 ▼ |
|---|---|---|---|---|---|
| C0004238 | Atrial Fibrillation | CHGA | 1113 | chromogranin A | P10645 |
| C0524620 | Metabolic Syndrome X | CHGA | 1113 | chromogranin A | P10645 |
| C0022104 | Irritable Bowel Syndrome | CHGA | 1113 | chromogranin A | P10645 |
| C0003850 | Arteriosclerosis | CHGA | 1113 | chromogranin A | P10645 |
| C0017154 | Gastritis, Atrophic | CHGA | 1113 | chromogranin A | P10645 |
| C0206686 | Adrenocortical carcinoma | CHGA | 1113 | chromogranin A | P10645 |
| C0007138 | Carcinoma, Transitional Cell | CHGA | 1113 | chromogranin A | P10645 |
| C0699790 | Colon Carcinoma | CHGA | 1113 | chromogranin A | P10645 |
| C0002965 | Angina, Unstable | CHGA | 1113 | chromogranin A | P10645 |
| C0262584 | Carcinoma, Small Cell | CHGA | 1113 | chromogranin A | P10645 |
| C0003469 | Anxiety Disorders | CHGA | 1113 | chromogranin A | P10645 |
| C0031941 | Pineal Gland Neoplasm | CHGA | 1113 | chromogranin A | P10645 |
| C0017661 | IGA Glomerulonephritis | CHGA | 1113 | chromogranin A | P10645 |
| C0014070 | Encephalomyelitis | CHGA | 1113 | chromogranin A | P10645 |
| C0001430 | Adenoma | CHGA | 1113 | chromogranin A | P10645 |
| C0017150 | Gastrinoma | CHGA | 1113 | chromogranin A | P10645 |
| C1565489 | Renal Insufficiency | CHGA | 1113 | chromogranin A | P10645 |
| C0029408 | Degenerative polyarthritis | CHGA | 1113 | chromogranin A | P10645 |
| C0020615 | Hypoglycemia | CHGA | 1113 | chromogranin A | P10645 |
| C0013395 | Dyspepsia | CHGA | 1113 | chromogranin A | P10645 |
| C0027651 | Neoplasms | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0024530 | Malaria | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0006142 | Malignant neoplasm of breast | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0678222 | Breast Carcinoma | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C1956346 | Coronary Artery Disease | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
