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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 ▲ |
|---|---|---|---|---|---|
| C0017636 | Glioblastoma | PLPP3 | 8613 | phospholipid phosphatase 3 | O14495 |
| C1956346 | Coronary Artery Disease | PLPP3 | 8613 | phospholipid phosphatase 3 | O14495 |
| C0010054 | Coronary Arteriosclerosis | PLPP3 | 8613 | phospholipid phosphatase 3 | O14495 |
| C0018801 | Heart failure | PLPP3 | 8613 | phospholipid phosphatase 3 | O14495 |
| C0006826 | Malignant Neoplasms | PLPP3 | 8613 | phospholipid phosphatase 3 | O14495 |
| C0007222 | Cardiovascular Diseases | PLPP3 | 8613 | phospholipid phosphatase 3 | O14495 |
| C0278878 | Adult Glioblastoma | PLPP3 | 8613 | phospholipid phosphatase 3 | O14495 |
| C0027051 | Myocardial Infarction | PLPP3 | 8613 | phospholipid phosphatase 3 | O14495 |
| C1842247 | CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 | PLPP3 | 8613 | phospholipid phosphatase 3 | O14495 |
| C0009375 | Colonic Neoplasms | PLPP3 | 8613 | phospholipid phosphatase 3 | O14495 |
| C0018802 | Congestive heart failure | PLPP3 | 8613 | phospholipid phosphatase 3 | O14495 |
| C0038454 | Cerebrovascular accident | PLPP3 | 8613 | phospholipid phosphatase 3 | O14495 |
| C0948008 | Ischemic stroke | PLPP3 | 8613 | phospholipid phosphatase 3 | O14495 |
| C1306459 | Primary malignant neoplasm | PLPP3 | 8613 | phospholipid phosphatase 3 | O14495 |
| C1621958 | Glioblastoma Multiforme | PLPP3 | 8613 | phospholipid phosphatase 3 | O14495 |
| C0031511 | Pheochromocytoma | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
| C0030421 | Paraganglioma | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
| C0027651 | Neoplasms | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
| C3888391 | Nonnuclear polymorphic congenital cataract | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
| C1265996 | Large cell neuroendocrine carcinoma | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
| C1868633 | Paragangliomas with Sensorineural Hearing Loss | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
| C0238198 | Gastrointestinal Stromal Tumors | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
| C1847319 | PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
| C0019562 | Von Hippel-Lindau Syndrome | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
| C0206667 | Adrenal Cortical Adenoma | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
