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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 |
|---|---|---|---|---|---|
| C0030421 | Paraganglioma | CHGA | 1113 | chromogranin A | P10645 |
| C0206663 | Neuroectodermal Tumor, Primitive | CHGA | 1113 | chromogranin A | P10645 |
| C0005695 | Bladder Neoplasm | CHGA | 1113 | chromogranin A | P10645 |
| C0149925 | Small cell carcinoma of lung | CHGA | 1113 | chromogranin A | P10645 |
| C0022661 | Kidney Failure, Chronic | CHGA | 1113 | chromogranin A | P10645 |
| C0027051 | Myocardial Infarction | CHGA | 1113 | chromogranin A | P10645 |
| C0238067 | Colitis, Collagenous | CHGA | 1113 | chromogranin A | P10645 |
| C0002736 | Amyotrophic Lateral Sclerosis | CHGA | 1113 | chromogranin A | P10645 |
| C0021390 | Inflammatory Bowel Diseases | CHGA | 1113 | chromogranin A | P10645 |
| C0700095 | Central neuroblastoma | CHGA | 1113 | chromogranin A | P10645 |
| C0033578 | Prostatic Neoplasms | CHGA | 1113 | chromogranin A | P10645 |
| C1857276 | Trichohepatoenteric Syndrome | CHGA | 1113 | chromogranin A | P10645 |
| C0400822 | Colitis, Lymphocytic | CHGA | 1113 | chromogranin A | P10645 |
| C0006142 | Malignant neoplasm of breast | CHGA | 1113 | chromogranin A | P10645 |
| C0007102 | Malignant tumor of colon | CHGA | 1113 | chromogranin A | P10645 |
| C0027719 | Nephrosclerosis | CHGA | 1113 | chromogranin A | P10645 |
| C0206695 | Carcinoma, Neuroendocrine | CHGA | 1113 | chromogranin A | P10645 |
| C1332206 | Adult Lymphoma | CHGA | 1113 | chromogranin A | P10645 |
| C0848548 | hypertensive nephropathy | CHGA | 1113 | chromogranin A | P10645 |
| C0031511 | Pheochromocytoma | CHGA | 1113 | chromogranin A | P10645 |
| C1336878 | Ureter Small Cell Carcinoma | CHGA | 1113 | chromogranin A | P10645 |
| C0019562 | Von Hippel-Lindau Syndrome | CHGA | 1113 | chromogranin A | P10645 |
| C0279988 | Childhood Angiosarcoma | CHGA | 1113 | chromogranin A | P10645 |
| C0699791 | Stomach Carcinoma | CHGA | 1113 | chromogranin A | P10645 |
| C0007137 | Squamous cell carcinoma | CHGA | 1113 | chromogranin A | P10645 |
