Celiac disease
Celiac disease
Definition
An autoimmune genetic disorder with an unknown pattern of inheritance that primarily affects the digestive tract. It is caused by intolerance to dietary gluten. Consumption of gluten protein triggers an immune response which damages small intestinal villi and prevents adequate absorption of nutrients. Clinical signs include abdominal cramping, diarrhea or constipation and weight loss. If untreated, the clinical course may progress to malnutrition, anemia, osteoporosis and an increased risk of intestinal malignancies. However, the prognosis is favorable with successful avoidance of gluten in the diet.
Also known as celiac disease, celiac sprue, coeliac sprue, gluten intolerance, gluten-induced enteropathy, non tropical sprue — per MONDO
Also identified as
- DOID 10608 per MONDO
- ICD10CM K90.0 per MONDO
- ICD9 579.0 per MONDO
- MESH D002446 per MONDO
- NCIT C26714 per MONDO
- Orphanet 555 per MONDO
- SCTID 396331005 per MONDO
- UMLS C0007570 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Alimentary part of gastrointestinal system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Alimentary part of gastrointestinal system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Intestine | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Intestine | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Small intestine | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Small intestine | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |