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 40001 - 40025 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0011848 Diabetes Insipidus GLB1 2720 galactosidase beta 1 P16278
C0020473 Hyperlipidemia GLB1 2720 galactosidase beta 1 P16278
C0426970 Spastic Quadriplegia GLB1 2720 galactosidase beta 1 P16278
C0022661 Kidney Failure, Chronic GLB1 2720 galactosidase beta 1 P16278
C0279680 Transitional cell carcinoma of bladder GLB1 2720 galactosidase beta 1 P16278
C0028754 Obesity PNLIP 5406 pancreatic lipase P16233
C0024523 Malabsorption Syndrome PNLIP 5406 pancreatic lipase P16233
C0017638 Glioma PNLIP 5406 pancreatic lipase P16233
C0011860 Diabetes Mellitus, Non-Insulin-Dependent PNLIP 5406 pancreatic lipase P16233
C0030305 Pancreatitis PNLIP 5406 pancreatic lipase P16233
C0027651 Neoplasms PNLIP 5406 pancreatic lipase P16233
C0346647 Malignant neoplasm of pancreas PNLIP 5406 pancreatic lipase P16233
C0040034 Thrombocytopenia PNLIP 5406 pancreatic lipase P16233
C0023467 Leukemia, Myelocytic, Acute PNLIP 5406 pancreatic lipase P16233
C0001339 Acute pancreatitis PNLIP 5406 pancreatic lipase P16233
C0235974 Pancreatic carcinoma PNLIP 5406 pancreatic lipase P16233
C0038238 Steatorrhea PNLIP 5406 pancreatic lipase P16233
C0342783 Deficiency of butyryl-CoA dehydrogenase ACADS 35 acyl-CoA dehydrogenase short chain P16219
C0027651 Neoplasms ACADS 35 acyl-CoA dehydrogenase short chain P16219
C0010054 Coronary Arteriosclerosis ACADS 35 acyl-CoA dehydrogenase short chain P16219
C0018801 Heart failure ACADS 35 acyl-CoA dehydrogenase short chain P16219
C0235527 Heart Failure, Right-Sided ACADS 35 acyl-CoA dehydrogenase short chain P16219
C0235974 Pancreatic carcinoma ACADS 35 acyl-CoA dehydrogenase short chain P16219
C0026848 Myopathy ACADS 35 acyl-CoA dehydrogenase short chain P16219
C0032897 Prader-Willi Syndrome ACADS 35 acyl-CoA dehydrogenase short chain P16219

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Last updated: August 19, 2024