DA90.1 Congenital intestinal transport defect
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
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.
code elsewhere
- Glucose-galactose malabsorption (5C61.0)
- Fructose malabsorption (5C61.40)
- Acrodermatitis enteropathica (5C64.20)
- Idiopathic bile acid malabsorption (DA96.02)
- Hereditary megaloblastic anaemia due to transcobalamin deficiency (3A01.0)
- Glycogen storage disease due to GLUT2 deficiency (5C51.3)
- Lysinuric protein intolerance (5C60.Y)
- Haptocorrin deficiency (5C63.0)
- Hereditary folate malabsorption (5C63.1)
- Vitamin B12 deficiency anaemia due to selective vitamin B12 malabsorption with proteinuria (3A01.Y)
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed
synonyms
- Congenital intestinal transport defect
- Congenital chloride diarrhoea
- Congenital sodium diarrhoea
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