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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

synonyms

• Congenital intestinal transport defect
• Congenital chloride diarrhoea
• Congenital sodium diarrhoea

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