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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 |
|---|---|---|---|---|---|
| C0005684 | Malignant neoplasm of urinary bladder | CHGA | 1113 | chromogranin A | P10645 |
| C0011991 | Diarrhea | CHGA | 1113 | chromogranin A | P10645 |
| C0027819 | Neuroblastoma | CHGA | 1113 | chromogranin A | P10645 |
| C0001418 | Adenocarcinoma | CHGA | 1113 | chromogranin A | P10645 |
| C1335302 | Pancreatic Ductal Adenocarcinoma | CHGA | 1113 | chromogranin A | P10645 |
| C0031099 | Periodontitis | CHGA | 1113 | chromogranin A | P10645 |
| C0006826 | Malignant Neoplasms | CHGA | 1113 | chromogranin A | P10645 |
| C0007097 | Carcinoma | CHGA | 1113 | chromogranin A | P10645 |
| C0024115 | Lung diseases | CHGA | 1113 | chromogranin A | P10645 |
| C0011849 | Diabetes Mellitus | CHGA | 1113 | chromogranin A | P10645 |
| C1332979 | Childhood Lymphoma | CHGA | 1113 | chromogranin A | P10645 |
| C1306459 | Primary malignant neoplasm | CHGA | 1113 | chromogranin A | P10645 |
| C0796074 | MOHR-TRANEBJAERG SYNDROME | CHGA | 1113 | chromogranin A | P10645 |
| C0403447 | Chronic Kidney Insufficiency | CHGA | 1113 | chromogranin A | P10645 |
| C0011847 | Diabetes | CHGA | 1113 | chromogranin A | P10645 |
| C0013595 | Eczema | CHGA | 1113 | chromogranin A | P10645 |
| C0020538 | Hypertensive disease | CHGA | 1113 | chromogranin A | P10645 |
| C0206667 | Adrenal Cortical Adenoma | CHGA | 1113 | chromogranin A | P10645 |
| C0022336 | Creutzfeldt-Jakob disease | CHGA | 1113 | chromogranin A | P10645 |
| C0678222 | Breast Carcinoma | CHGA | 1113 | chromogranin A | P10645 |
| C0014859 | Esophageal Neoplasms | CHGA | 1113 | chromogranin A | P10645 |
| C2882221 | Acute pulmonary embolism | CHGA | 1113 | chromogranin A | P10645 |
| C1956346 | Coronary Artery Disease | CHGA | 1113 | chromogranin A | P10645 |
| C0026769 | Multiple Sclerosis | CHGA | 1113 | chromogranin A | P10645 |
| C0018801 | Heart failure | CHGA | 1113 | chromogranin A | P10645 |
