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 ▲ |
---|---|---|---|---|---|
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