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 876 - 900 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0004114 Astrocytoma PFKFB4 5210 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 Q16877
C0149925 Small cell carcinoma of lung PFKFB4 5210 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 Q16877
C1514422 Glioblastoma, IDH-Wildtype PFKFB4 5210 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 Q16877
C0017636 Glioblastoma PFKFB4 5210 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 Q16877
C0025202 melanoma PFKFB4 5210 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 Q16877
C1458155 Mammary Neoplasms PFKFB4 5210 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 Q16877
C0024530 Malaria PGLS 25796 6-phosphogluconolactonase O95336
C0029459 Osteoporosis, Senile PGLS 25796 6-phosphogluconolactonase O95336
C0751406 Post-Traumatic Osteoporosis PGLS 25796 6-phosphogluconolactonase O95336
C0006142 Malignant neoplasm of breast PGLS 25796 6-phosphogluconolactonase O95336
C3642345 Luminal A Breast Carcinoma PGLS 25796 6-phosphogluconolactonase O95336
C0001787 Osteoporosis, Age-Related PGLS 25796 6-phosphogluconolactonase O95336
C0029456 Osteoporosis PGLS 25796 6-phosphogluconolactonase O95336
C0678222 Breast Carcinoma PGLS 25796 6-phosphogluconolactonase O95336
C2713347 7-Dehydrocholesterol Reductase Deficiency DHCR7 1717 7-dehydrocholesterol reductase Q9UBM7
C0175694 Smith-Lemli-Opitz Syndrome DHCR7 1717 7-dehydrocholesterol reductase Q9UBM7
C0036439 Scoliosis, unspecified DHCR7 1717 7-dehydrocholesterol reductase Q9UBM7
C3696376 3-Methylglutaconic Aciduria DHCR7 1717 7-dehydrocholesterol reductase Q9UBM7
C0026650 Movement Disorders DHCR7 1717 7-dehydrocholesterol reductase Q9UBM7
C0239946 Fibrosis, Liver DHCR7 1717 7-dehydrocholesterol reductase Q9UBM7
C2717836 Steroid Sulfatase Deficiency Disease DHCR7 1717 7-dehydrocholesterol reductase Q9UBM7
C0000768 Congenital Abnormality DHCR7 1717 7-dehydrocholesterol reductase Q9UBM7
C0398739 Congenital disorder of glycosylation, type 2C DHCR7 1717 7-dehydrocholesterol reductase Q9UBM7
C0011860 Diabetes Mellitus, Non-Insulin-Dependent DHCR7 1717 7-dehydrocholesterol reductase Q9UBM7
C0017601 Glaucoma DHCR7 1717 7-dehydrocholesterol reductase Q9UBM7

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