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
Displaying entries 39626 - 39650 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
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