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MIRAGE
congenital sucrase-isomaltase deficiency
Summary
- Synonym
-
- CSID
- SI deficiency
- congenital sucrase-isomaltose malabsorption
- congenital sucrose intolerance
- disaccharide intolerance
- Definition
- A carbohydrate metabolic disorder characterized by malabsorption of oligosaccharides and disaccharides that has_material_basis_in homozygous or compound heterozygous mutation in SI on chromosome 3q26.1.
- Super Class
- autosomal recessive disease carbohydrate metabolic disorder physical disorder
External Links
- Disease Ontology
- DOID:0111633
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- ORDO
- GARD
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P14410 | Sucrase-isomaltase, intestinal |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002607 | Bowel incontinence |
| HP:0002018 | Nausea |
| HP:0012378 | Fatigue |
| HP:0002013 | Vomiting |
| HP:0004396 | Poor appetite |
| HP:0002020 | Gastroesophageal reflux |
| HP:0001508 | Failure to thrive |
| HP:0003270 | Abdominal distention |
| HP:0002019 | Constipation |
| HP:0011848 | Abdominal colic |
