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 ▼ |
---|---|---|---|---|---|
C0022951 | Lactose Intolerance | LCT | 3938 | lactase | P09848 |
C0268181 | Lactose Intolerance, Adult Type | LCT | 3938 | lactase | P09848 |
C0028754 | Obesity | LCT | 3938 | lactase | P09848 |
C1956346 | Coronary Artery Disease | LCT | 3938 | lactase | P09848 |
C0524620 | Metabolic Syndrome X | LCT | 3938 | lactase | P09848 |
C0006826 | Malignant Neoplasms | LCT | 3938 | lactase | P09848 |
C0432306 | Ichthyosis Bullosa of Siemens | LCT | 3938 | lactase | P09848 |
C0036341 | Schizophrenia | LCT | 3938 | lactase | P09848 |
C0027651 | Neoplasms | LCT | 3938 | lactase | P09848 |
C0032580 | Adenomatous Polyposis Coli | LCT | 3938 | lactase | P09848 |
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 |
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Last updated: August 19, 2024