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Results 1 - 4 of 4 for Malabsorption
  1. SLC46A1 gene 
    ... have been identified in people with hereditary folate malabsorption. This disorder interferes with the body's ability ... and other signs and symptoms of hereditary folate malabsorption. More About This Health Condition HCP1 heme carrier ...
    https://medlineplus.gov/genetics/gene/slc46a1 - Genetics
  2. SLC5A1 gene 
    ... gene have been found to cause glucose-galactose malabsorption. This condition begins in infancy and is characterized ... present at all, in people with glucose-galactose malabsorption. More About This Health Condition D22S675 Human Na+/ ...
    https://medlineplus.gov/genetics/gene/slc5a1 - Genetics
  3. SAR1B gene 
    ... bloodstream. Impaired chylomicron transport causes severely decreased absorption (malabsorption) of dietary fats and fat-soluble vitamins, leading ...
    https://medlineplus.gov/genetics/gene/sar1b - Genetics
  4. SI gene 
    ... sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption. Hum Mutat. 2006 Jan;27(1):119. doi: ...
    https://medlineplus.gov/genetics/gene/si - Genetics