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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 |
|---|---|---|---|---|---|
| C1458155 | Mammary Neoplasms | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
| C0013274 | Patent ductus arteriosus | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
| C0011884 | Diabetic Retinopathy | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
| C0153567 | Uterine Cancer | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
| C0029456 | Osteoporosis | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
| C0028754 | Obesity | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
| C0022408 | Arthropathy | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
| C1956390 | Cranial Arteritis | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
| C0015674 | Chronic Fatigue Syndrome | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
| C0040128 | Thyroid Diseases | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
| C1956346 | Coronary Artery Disease | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0282577 | Congenital Disorders of Glycosylation | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0023895 | Liver diseases | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0011849 | Diabetes Mellitus | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0555198 | Malignant Glioma | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C1865145 | Congenital disorder of glycosylation type 1B | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0010068 | Coronary heart disease | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0311276 | Severe malnutrition | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0036341 | Schizophrenia | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0007222 | Cardiovascular Diseases | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0033680 | Protein-Losing Enteropathies | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0342881 | Familial hypercholesterolemia - homozygous | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0018801 | Heart failure | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0038436 | Post-Traumatic Stress Disorder | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0040580 | Tracheal Diseases | MPI | 4351 | mannose phosphate isomerase | P34949 |
