Congenital bile acid synthesis defect 2

MONDO:0009339

Congenital bile acid synthesis defect type 2 (BAS defect type 2) is an anomaly of bile acid synthesis characterized by severe and rapidly progressive cholestatic liver disease, and malabsorption of fat and fat-soluble vitamins.

Also known as: AKR1D1 congenital bile acid synthesis defect, BASD2, CBAS2, bile acid synthesis defect, congenital, type 2, cholestasis with delta(4)-3-oxosteroid 5-beta-reductase deficiency, congenital bile acid synthesis defect caused by mutation in AKR1D1, congenital bile acid synthesis defect type 2, bile acid synthesis defect, congenital, 2

35 clinical trials for this condition and its sub-types.

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