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 48151 - 48175 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0038356 Stomach Neoplasms UPP1 7378 uridine phosphorylase 1 Q16831
C0040136 Thyroid Neoplasm UPP1 7378 uridine phosphorylase 1 Q16831
C0006826 Malignant Neoplasms UPP1 7378 uridine phosphorylase 1 Q16831
C0024623 Malignant neoplasm of stomach UPP1 7378 uridine phosphorylase 1 Q16831
C0345964 Adenoma of lung UPP1 7378 uridine phosphorylase 1 Q16831
C0006142 Malignant neoplasm of breast UPP1 7378 uridine phosphorylase 1 Q16831
C0279626 Squamous cell carcinoma of esophagus UPP1 7378 uridine phosphorylase 1 Q16831
C0162820 Dermatitis, Allergic Contact UPP1 7378 uridine phosphorylase 1 Q16831
C0011849 Diabetes Mellitus UPP1 7378 uridine phosphorylase 1 Q16831
C1319315 Adenocarcinoma of large intestine UPP1 7378 uridine phosphorylase 1 Q16831
C0011847 Diabetes UPP1 7378 uridine phosphorylase 1 Q16831
C0699791 Stomach Carcinoma UPP1 7378 uridine phosphorylase 1 Q16831
C0015934 Fetal Growth Retardation UPP1 7378 uridine phosphorylase 1 Q16831
C0017536 Giardiasis UPP1 7378 uridine phosphorylase 1 Q16831
C0549473 Thyroid carcinoma UPP1 7378 uridine phosphorylase 1 Q16831
C0014518 Toxic Epidermal Necrolysis UPP1 7378 uridine phosphorylase 1 Q16831
C0041296 Tuberculosis UPP1 7378 uridine phosphorylase 1 Q16831
C0011884 Diabetic Retinopathy UPP1 7378 uridine phosphorylase 1 Q16831
C1864948 Hyperinsulinemic Hypoglycemia, Familial, 4 HADH 3033 hydroxyacyl-CoA dehydrogenase Q16836
C0028754 Obesity HADH 3033 hydroxyacyl-CoA dehydrogenase Q16836
C0018801 Heart failure HADH 3033 hydroxyacyl-CoA dehydrogenase Q16836
C1291230 3-Hydroxyacyl-CoA Dehydrogenase Deficiency HADH 3033 hydroxyacyl-CoA dehydrogenase Q16836
C0220994 Hyperammonemia HADH 3033 hydroxyacyl-CoA dehydrogenase Q16836
C3888018 Congenital Hyperinsulinism HADH 3033 hydroxyacyl-CoA dehydrogenase Q16836
C0020617 Hypoglycemic coma HADH 3033 hydroxyacyl-CoA dehydrogenase Q16836

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Last updated: August 19, 2024