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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 |
|---|---|---|---|---|---|
| C1561643 | Chronic Kidney Diseases | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C1306459 | Primary malignant neoplasm | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0027651 | Neoplasms | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0559469 | Allergy to eggs | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0010414 | Infection by Cryptococcus neoformans | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C1861922 | CAMPOMELIC DYSPLASIA | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0005779 | Blood Coagulation Disorders | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C3888018 | Congenital Hyperinsulinism | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0221074 | Depression, Postpartum | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0349653 | Congenital disorder of glycosylation type 1A | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C1852502 | CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0023467 | Leukemia, Myelocytic, Acute | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0003467 | Anxiety | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0400966 | Non-alcoholic Fatty Liver Disease | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0024523 | Malabsorption Syndrome | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C1458140 | Bleeding tendency | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0002395 | Alzheimer's Disease | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0020459 | Hyperinsulinism | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0272375 | Antithrombin III Deficiency | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0003469 | Anxiety Disorders | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0007102 | Malignant tumor of colon | MRC1 | 4360 | mannose receptor C-type 1 | P22897 |
| C0032580 | Adenomatous Polyposis Coli | MRC1 | 4360 | mannose receptor C-type 1 | P22897 |
| C4552100 | Lynch Syndrome | MRC1 | 4360 | mannose receptor C-type 1 | P22897 |
| C1333990 | Hereditary Nonpolyposis Colorectal Cancer | MRC1 | 4360 | mannose receptor C-type 1 | P22897 |
| C0009447 | Common Variable Immunodeficiency | MRC1 | 4360 | mannose receptor C-type 1 | P22897 |
