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diarrhea
Summary
- Definition
- A gastrointestinal system disease described as the condition of having frequent loose or liquid bowel movements. Acute diarrhea is a common cause of death in developing countries and the second most common cause of infant deaths worldwide. The loss of fluids through diarrhea can cause severe dehydration which is one cause of death in diarrhea sufferers. Along with water, sufferers also lose dangerous amounts of important salts, electrolytes, and other nutrients. There are at least four types of diarrhea: secretory diarrhea, osmotic diarrhea, motility-related diarrhea, and inflammatory diarrhea.
- Super Class
- gastrointestinal system disease
External Links
- Disease Ontology
- DOID:13250
- Mondo Disease Ontology
- MeSH
- UMLS
- WikiPathways (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 1374 | CPT1A | carnitine palmitoyltransferase 1A | |
| 1544 | CYP1A2 | cytochrome P450 family 1 subfamily A member 2 | |
| 1557 | CYP2C19 | cytochrome P450 family 2 subfamily C member 19 | |
| 1559 | CYP2C9 | cytochrome P450 family 2 subfamily C member 9 | |
| 1576 | CYP3A4 | cytochrome P450 family 3 subfamily A member 4 | |
| 1581 | CYP7A1 | cytochrome P450 family 7 subfamily A member 1 | |
| 1585 | CYP11B2 | cytochrome P450 family 11 subfamily B member 2 | |
| 1593 | CYP27A1 | cytochrome P450 family 27 subfamily A member 1 | |
| 1604 | CD55 | CD55 molecule (Cromer blood group) | |
| 1836 | SLC26A2 | solute carrier family 26 member 2 |
Related Glycoprotein
