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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 ▲ |
|---|---|---|---|---|---|
| C0037926 | Compression of spinal cord | MINPP1 | 9562 | multiple inositol-polyphosphate phosphatase 1 | Q9UNW1 |
| C0018023 | Nodular Goiter | MINPP1 | 9562 | multiple inositol-polyphosphate phosphatase 1 | Q9UNW1 |
| C0018671 | Head and Neck Neoplasms | MINPP1 | 9562 | multiple inositol-polyphosphate phosphatase 1 | Q9UNW1 |
| C3501843 | Nonmedullary Thyroid Carcinoma | MINPP1 | 9562 | multiple inositol-polyphosphate phosphatase 1 | Q9UNW1 |
| C0019196 | Hepatitis C | PLA2G4C | 8605 | phospholipase A2 group IVC | Q9UP65 |
| C0003850 | Arteriosclerosis | PLA2G4C | 8605 | phospholipase A2 group IVC | Q9UP65 |
| C0017638 | Glioma | PLA2G4C | 8605 | phospholipase A2 group IVC | Q9UP65 |
| C0027651 | Neoplasms | PLA2G4C | 8605 | phospholipase A2 group IVC | Q9UP65 |
| C1510586 | Autism Spectrum Disorders | PLA2G4C | 8605 | phospholipase A2 group IVC | Q9UP65 |
| C0036341 | Schizophrenia | PLA2G4C | 8605 | phospholipase A2 group IVC | Q9UP65 |
| C0751396 | Well Differentiated Oligodendroglioma | PLA2G4C | 8605 | phospholipase A2 group IVC | Q9UP65 |
| C0004096 | Asthma | PLA2G4C | 8605 | phospholipase A2 group IVC | Q9UP65 |
| C0334590 | Anaplastic Oligodendroglioma | PLA2G4C | 8605 | phospholipase A2 group IVC | Q9UP65 |
| C0006142 | Malignant neoplasm of breast | PLA2G4C | 8605 | phospholipase A2 group IVC | Q9UP65 |
| C0024117 | Chronic Obstructive Airway Disease | PLA2G4C | 8605 | phospholipase A2 group IVC | Q9UP65 |
| C0282577 | Congenital Disorders of Glycosylation | COG5 | 10466 | component of oligomeric golgi complex 5 | Q9UP83 |
| C3714756 | Intellectual Disability | COG5 | 10466 | component of oligomeric golgi complex 5 | Q9UP83 |
| C0520947 | Clumsiness - motor delay | COG5 | 10466 | component of oligomeric golgi complex 5 | Q9UP83 |
| C0010417 | Cryptorchidism | COG5 | 10466 | component of oligomeric golgi complex 5 | Q9UP83 |
| C1956346 | Coronary Artery Disease | COG5 | 10466 | component of oligomeric golgi complex 5 | Q9UP83 |
| C3150876 | COG5 congenital disorder of glycosylation | COG5 | 10466 | component of oligomeric golgi complex 5 | Q9UP83 |
| C0004238 | Atrial Fibrillation | COG5 | 10466 | component of oligomeric golgi complex 5 | Q9UP83 |
| C0235480 | Paroxysmal atrial fibrillation | COG5 | 10466 | component of oligomeric golgi complex 5 | Q9UP83 |
| C0016719 | Friedreich Ataxia | COG5 | 10466 | component of oligomeric golgi complex 5 | Q9UP83 |
| C0036572 | Seizures | COG5 | 10466 | component of oligomeric golgi complex 5 | Q9UP83 |
