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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID ▼ | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0011991 | Diarrhea | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0023903 | Liver neoplasms | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0014175 | Endometriosis | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0001925 | Albuminuria | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0085215 | Ovarian Failure, Premature | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0023895 | Liver diseases | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C3714756 | Intellectual Disability | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C4721610 | Carcinoma, Ovarian Epithelial | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0086543 | Cataract | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0025517 | Metabolic Diseases | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0020615 | Hypoglycemia | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0341858 | Endometriosis of uterus | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0751161 | UDPglucose 4-epimerase deficiency disease | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0919267 | ovarian neoplasm | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0002878 | Anemia, Hemolytic | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0025521 | Inborn Errors of Metabolism | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C1140680 | Malignant neoplasm of ovary | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0948896 | Primary hypogonadism | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C1458140 | Bleeding tendency | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0243026 | Sepsis | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0162429 | Malnutrition | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0022353 | Neonatal Jaundice | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0152259 | Cataract secondary to ocular disorder | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0027651 | Neoplasms | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0268155 | Deficiency of galactokinase | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
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Last updated: August 19, 2024