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GTR Home > Conditions/Phenotypes > Bile acid malabsorption, primary, 1

Summary

Primary bile acid malabsorption (PBAM) is an intestinal disorder associated with chronic watery diarrhea, excess fecal bile acids, and steatorrhea. Bile acid malabsorption has been classified into 3 main types depending on the etiology. Types 1 and 3 are secondary disorders: type 1 is due to ileal dysfunction resulting from Crohn disease or ileal resection, and type 3 is secondary to other conditions, including cholecystectomy, post-vagotomy, celiac disease, and pancreatic insufficiency. Type 2 bile acid malabsorption is a primary congenital disorder, including the rare type due to mutations in the SLC10A2 gene (review by Pattni and Walters, 2009). Genetic Heterogeneity of Primary Bile Acid Malabsorption Also see PBAM2 (619481), caused by mutation in the SLC51B gene (612085). [from OMIM]

Available tests

17 tests are in the database for this condition.

Genes See tests for all associated and related genes

  • Also known as: ASBT, IBAT, ISBT, NTCP2, PBAM, PBAM1, SLC10A2
    Summary: solute carrier family 10 member 2

Clinical features

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