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disaccharide malabsorption
(phenotype)
Summary
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Genetic Markers
Most Correlated Genes
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SI
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
Glycosyl hydrolases family 31, conserved site
Galactose mutarotase, N-terminal barrel
Glycosyl hydrolases family 31, active site
alpha-glucosidase activity
Glycoside hydrolase family 31
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OMIM - Specific enzyme deficiency
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Most Relevant Literature
The child with chronic diarrhoea: suggestions for workup].
Moderate disaccharide malabsorption does not affect weight gain and cecal cell proliferation in pigl…
Disaccharide intolerance].
Impaired trafficking and subcellular localization of a mutant lactase associated with congenital lac…
The prevalence and severity of intestinal disaccharidase deficiency in human immunodeficiency virus-…
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Most Relevant Clinical Trials
Efficacy of a Low FODMAP Diet in the Absence of Lactose Malabsorption in Moderate to Severe ROME IV …
Clinical Utility of Breath Tests in GI
Whole Milk Intake and Cardio-metabolic Risk Factors
Lactose and Lipids
Integrative Approaches to Managing Irritable Bowel Syndrome (IBS)
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