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 6126 - 6150 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0036572 Seizures SLC39A8 64116 solute carrier family 39 member 8 Q9C0K1
C0003850 Arteriosclerosis SLC39A8 64116 solute carrier family 39 member 8 Q9C0K1
C0023264 Leigh Disease SLC39A8 64116 solute carrier family 39 member 8 Q9C0K1
C0006142 Malignant neoplasm of breast SLC39A8 64116 solute carrier family 39 member 8 Q9C0K1
C0268146 Glucose-6-phosphate transport defect SLC37A4 2542 solute carrier family 37 member 4 O43826
C0027947 Neutropenia SLC37A4 2542 solute carrier family 37 member 4 O43826
C0011849 Diabetes Mellitus SLC37A4 2542 solute carrier family 37 member 4 O43826
C0027651 Neoplasms SLC37A4 2542 solute carrier family 37 member 4 O43826
C0206624 Hepatoblastoma SLC37A4 2542 solute carrier family 37 member 4 O43826
C0025521 Inborn Errors of Metabolism SLC37A4 2542 solute carrier family 37 member 4 O43826
C0017919 Glycogen Storage Disease SLC37A4 2542 solute carrier family 37 member 4 O43826
C0342749 GLYCOGEN STORAGE DISEASE Ic SLC37A4 2542 solute carrier family 37 member 4 O43826
C1853118 Severe congenital neutropenia SLC37A4 2542 solute carrier family 37 member 4 O43826
C0028754 Obesity SLC37A4 2542 solute carrier family 37 member 4 O43826
C0017668 Focal glomerulosclerosis SLC37A4 2542 solute carrier family 37 member 4 O43826
C0017920 Glycogen Storage Disease Type I SLC37A4 2542 solute carrier family 37 member 4 O43826
C0032460 Polycystic Ovary Syndrome SLC37A4 2542 solute carrier family 37 member 4 O43826
C0001125 Acidosis, Lactic SLC37A4 2542 solute carrier family 37 member 4 O43826
C0023530 Leukopenia SLC37A4 2542 solute carrier family 37 member 4 O43826
C0017495 Gerstmann-Straussler-Scheinker Disease SLC37A4 2542 solute carrier family 37 member 4 O43826
C0013336 Dwarfism SLC37A4 2542 solute carrier family 37 member 4 O43826
C0025517 Metabolic Diseases SLC37A4 2542 solute carrier family 37 member 4 O43826
C2239176 Liver carcinoma SLC37A4 2542 solute carrier family 37 member 4 O43826
C0006118 Brain Neoplasms SLC37A4 2542 solute carrier family 37 member 4 O43826
C0278878 Adult Glioblastoma SLC37A4 2542 solute carrier family 37 member 4 O43826

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Last updated: August 19, 2024