Catalog
Congenital intestinal transport defect
Link to WHO Definition
Congenital intestinal transport defect – http://id.who.int/icd/entity/671778206
This is a congenital disease of the small intestinal mucosa that presents with intractable diarrhoea and malabsorption of nutrients in young children, due to defect of transporter of nutrients in enterocytes.
Parents
Children
- Haptocorrin deficiency
- Vitamin B12 deficiency anaemia due to selective vitamin B12 malabsorption with proteinuria
- 5C61.40 Fructose malabsorption
- Idiopathic bile acid malabsorption
- Congenital sodium diarrhoea
- 5C64.20 Acrodermatitis enteropathica
- 5C61.0 Glucose-galactose malabsorption
- Glycogen storage disease due to GLUT2 deficiency
- Congenital chloride diarrhoea
- Hereditary folate malabsorption
- Hereditary megaloblastic anaemia due to transcobalamin deficiency
- Lysinuric protein intolerance