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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 |
|---|---|---|---|
| 57124 | CD248 | CD248 molecule | |
| 79053 | ALG8 | ALG8 alpha-1,3-glucosyltransferase | |
| 79947 | DHDDS | dehydrodolichyl diphosphate synthase subunit | |
| 80270 | HSD3B7 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 | |
| 138050 | HGSNAT | heparan-alpha-glucosaminide N-acetyltransferase | |
| 152831 | KLB | klotho beta | |
| 197322 | ACSF3 | acyl-CoA synthetase family member 3 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P16442 | Histo-blood group ABO system transferase | |
| P16662 | UDP-glucuronosyltransferase 2B7 | |
| P17931 | Galectin-3 | |
| P19224 | UDP-glucuronosyltransferase 1-6 | |
| P19526 | Galactoside alpha-(1,2)-fucosyltransferase 1 | |
| P19971 | Thymidine phosphorylase | |
| P20933 | N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase | |
| P21964 | Catechol O-methyltransferase | |
| P22304 | Iduronate 2-sulfatase | |
| P22309 | UDP-glucuronosyltransferase 1A1 |
