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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 |
|---|---|---|---|---|---|
| C1956346 | Coronary Artery Disease | PLA2G2D | 26279 | phospholipase A2 group IID | Q9UNK4 |
| C0027651 | Neoplasms | PLA2G2D | 26279 | phospholipase A2 group IID | Q9UNK4 |
| C0010068 | Coronary heart disease | PLA2G2D | 26279 | phospholipase A2 group IID | Q9UNK4 |
| C0008311 | Cholangitis | PLA2G2D | 26279 | phospholipase A2 group IID | Q9UNK4 |
| C0003850 | Arteriosclerosis | PLA2G2D | 26279 | phospholipase A2 group IID | Q9UNK4 |
| C0024117 | Chronic Obstructive Airway Disease | PLA2G2D | 26279 | phospholipase A2 group IID | Q9UNK4 |
| C0013080 | Down Syndrome | PLA2G2D | 26279 | phospholipase A2 group IID | Q9UNK4 |
| C0007102 | Malignant tumor of colon | PLA2G2D | 26279 | phospholipase A2 group IID | Q9UNK4 |
| C0699790 | Colon Carcinoma | PLA2G2D | 26279 | phospholipase A2 group IID | Q9UNK4 |
| C1306459 | Primary malignant neoplasm | PLA2G2D | 26279 | phospholipase A2 group IID | Q9UNK4 |
| C0006826 | Malignant Neoplasms | PLA2G2D | 26279 | phospholipase A2 group IID | Q9UNK4 |
| C0023264 | Leigh Disease | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0027066 | Myoclonus | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0039685 | Tetralogy of Fallot | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0029408 | Degenerative polyarthritis | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0524851 | Neurodegenerative Disorders | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0085584 | Encephalopathies | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0038379 | Strabismus | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0025521 | Inborn Errors of Metabolism | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0013421 | Dystonia | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0027651 | Neoplasms | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0010417 | Cryptorchidism | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0036572 | Seizures | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0393593 | Dystonia Disorders | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0009402 | Colorectal Carcinoma | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
