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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 ▲ |
|---|---|---|---|---|---|
| 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 |
| C0010068 | Coronary heart disease | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C1956346 | Coronary Artery Disease | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0028754 | Obesity | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0009402 | Colorectal Carcinoma | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0036341 | Schizophrenia | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0745103 | Hyperlipoproteinemia Type IIa | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0019189 | Hepatitis, Chronic | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0342883 | Cholesteryl Ester Transfer Protein Deficiency | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0242383 | Age related macular degeneration | LIPC | 3990 | lipase C, hepatic type | P11150 |
