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 15876 - 15900 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0341106 Eosinophilic esophagitis LCT 3938 lactase P09848
C0017572 Gingival Recession LCT 3938 lactase P09848
C0009402 Colorectal Carcinoma LCT 3938 lactase P09848
C0032460 Polycystic Ovary Syndrome LCT 3938 lactase P09848
C0007570 Celiac Disease LCT 3938 lactase P09848
C0409974 Lupus Erythematosus LCT 3938 lactase P09848
C0272375 Antithrombin III Deficiency LCT 3938 lactase P09848
C0028768 Obsessive-Compulsive Disorder LCT 3938 lactase P09848
C0020538 Hypertensive disease LCT 3938 lactase P09848
C0085409 Polyendocrinopathies, Autoimmune LCT 3938 lactase P09848
C0029443 Osteomyelitis LCT 3938 lactase P09848
C0035319 Retinal Necrosis Syndrome, Acute LCT 3938 lactase P09848
C0009324 Ulcerative Colitis LCT 3938 lactase P09848
C0024138 Lupus Erythematosus, Discoid LCT 3938 lactase P09848
C0032285 Pneumonia LCT 3938 lactase P09848
C0600139 Prostate carcinoma LCT 3938 lactase P09848
C0023601 Leydig Cell Tumor LCT 3938 lactase P09848
C1851841 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 1 LCT 3938 lactase P09848
C0040517 Gilles de la Tourette syndrome LCT 3938 lactase P09848
C0011991 Diarrhea LCT 3938 lactase P09848
C0029456 Osteoporosis LCT 3938 lactase P09848
C0162429 Malnutrition LCT 3938 lactase P09848
C0220981 Metabolic acidosis LCT 3938 lactase P09848
C0010674 Cystic Fibrosis LCT 3938 lactase P09848
C0022104 Irritable Bowel Syndrome LCT 3938 lactase P09848

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Last updated: August 19, 2024