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Results 1 - 10 of 16 for Malabsorption
  1. Glucose-galactose malabsorption 
    Glucose-galactose malabsorption is a condition in which the body cannot take in (absorb) the sugars glucose and galactose, which primarily results in severe diarrhea. ...
    https://medlineplus.gov/.../glucose-galactose-malabsorption - Genetics
  2. Hereditary folate malabsorption 
    Hereditary folate malabsorption is a disorder that interferes with the body's ability to use certain vitamins from food. During digestion, ... and blood cell formation. Infants with hereditary folate malabsorption are born with normal amounts of folates in ...
    https://medlineplus.gov/.../hereditary-folate-malabsorption - Genetics
  3. Imerslund-Gräsbeck syndrome 
    ... Defect of enterocyte intrinsic factor receptor Enterocyte cobalamin malabsorption Imerslund-Grasbeck syndrome Juvenile pernicious anemia with proteinuria ...
    https://medlineplus.gov/.../condition/imerslund-grasbeck-syndrome - Genetics
  4. Lactose intolerance 
    ... some degree of lactose intolerance. Alactasia Hypolactasia Lactose malabsorption Milk sugar intolerance Genetic Testing Registry: Congenital lactase ... LT. Country, regional, and global estimates for lactose malabsorption in adults: a systematic review and meta-analysis. ...
    https://medlineplus.gov/genetics/condition/lactose-intolerance - Genetics
  5. 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
  6. 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
  7. Hereditary fructose intolerance 
    ... not be confused with a condition called fructose malabsorption. In people with fructose malabsorption, the cells of the intestine cannot absorb fructose ...
    https://medlineplus.gov/.../hereditary-fructose-intolerance - Genetics
  8. Lysosomal acid lipase deficiency 
    ... steatorrhea), and poor absorption of nutrients from food (malabsorption). In addition, affected infants often have calcium deposits ... of individuals with the later-onset form have malabsorption, diarrhea, vomiting, and steatorrhea. Individuals with this form ...
    https://medlineplus.gov/.../lysosomal-acid-lipase-deficiency - Genetics
  9. Congenital sucrase-isomaltase deficiency 
    ... the condition. Congenital sucrose intolerance Congenital sucrose-isomaltose malabsorption CSID Disaccharide intolerance I SI deficiency Sucrase-isomaltase ...
    https://medlineplus.gov/.../congenital-sucrase-isomaltase-deficiency - Genetics
  10. Bare lymphocyte syndrome type II 
    ... the infections, affected infants have difficulty absorbing nutrients (malabsorption), and they grow more slowly than their peers. ...
    https://medlineplus.gov/.../bare-lymphocyte-syndrome-type-ii - Genetics
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