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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name ▲ | UniProt ID |
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C0006826 | Malignant Neoplasms | MPI | 4351 | mannose phosphate isomerase | P34949 |
C4317295 | Congenital disorder of glycosylation type 1s | MPI | 4351 | mannose phosphate isomerase | P34949 |
C4317224 | Congenital disorder of glycosylation type 1q | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0151744 | Myocardial Ischemia | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0456909 | Blindness | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0239946 | Fibrosis, Liver | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0036572 | Seizures | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0017638 | Glioma | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0018802 | Congestive heart failure | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0011991 | Diarrhea | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0027051 | Myocardial Infarction | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0752124 | Spinocerebellar Ataxia Type 6 (disorder) | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0015934 | Fetal Growth Retardation | MPI | 4351 | mannose phosphate isomerase | P34949 |
C1449563 | Cardiomyopathy, Familial Idiopathic | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0040034 | Thrombocytopenia | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0010674 | Cystic Fibrosis | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0554101 | Villous atrophy | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0010054 | Coronary Arteriosclerosis | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0024236 | Lymphedema | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0013238 | Dry Eye Syndromes | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0020538 | Hypertensive disease | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0009714 | Hepatic Fibrosis, Congenital | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0019163 | Hepatitis B | MPI | 4351 | mannose phosphate isomerase | P34949 |
C0020615 | Hypoglycemia | MPI | 4351 | mannose phosphate isomerase | P34949 |
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Last updated: August 19, 2024