Coeliac diseaseCeliacOther Metabolites Mapped to 'Celiac disease'HMDB0000756 (Hexanoylcarnitine) HMDB0000688 (Isovalerylcarnitine) HMDB0000222 (Palmitoylcarnitine) HMDB0000824 (Propionylcarnitine) HMDB0000138 (Glycocholic acid) HMDB0002250 (Dodecanoylcarnitine) HMDB0000791 (Octanoylcarnitine) HMDB0002013 (Butyrylcarnitine) HMDB0000740 (Lactulose) HMDB0000848 (Stearoylcarnitine)
- HMDB0002366 (Tiglylcarnitine)
- Celiac disease
- An autoimmune disease of gastrointestinal tract that is caused by a reaction located in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe triticeae. the disease is associated with hla-dq gene. it has symptom abdominal pain, has symptom constipation, has symptom diarrhea, has symptom nausea and vomiting, and has symptom loss of appetite. (do).
- Parent Term
- Health condition
- Parent Definition
- A health effect that consists on short or long-term disease, condition, disorder, syndrome or constant abnormality.