Inborn disorder of bile acid synthesis
MONDO:0019218Anomalies of bile acid synthesis are a group of sterol metabolism disorders due to enzyme deficiencies of bile acid synthesis (BAS) in infants, children and adults, with variable manifestations that include cholestasis, neurological disease, and fat malabsorption. Nine inborn errors have been described, 7 of which lead to liver cholestasis.
Also known as: Bile Acid Synthesis Disorders, inborn bile acid biosynthetic process disorder, inborn error of bile acid biosynthetic process, rare inborn error of bile acid biosynthetic process, disorder of bile acid synthesis, inborn errors of bile acid synthesis
12 clinical trials for this condition and its sub-types, 2 tagged with Inborn disorder of bile acid synthesis itself.
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Sub-types of Inborn disorder of bile acid synthesis
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Cerebrotendinous xanthomatosis 6 trials
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Hypercholanemia, familial 0 trials
2 sub-types
- Hypercholanemia, familial 1 0 trials
- Hypercholanemia, familial, 2 0 trials
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Can a decade of real-world data refine treatment for rare bile acid disorders?
Knowledge-focused OngoingThis study is a patient registry that will follow people of any age with bile acid synthesis disorders who are treated with Cholbam (cholic acid). The goal is to collect information over 10 years on how the drug performs in routine clinical care, including its safety, effectivene…
Sponsor: Mirum Pharmaceuticals, Inc. • Aim: Knowledge-focused
Last updated Aug 02, 2026 00:00 UTC
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Major study on rare childhood liver diseases halted
Knowledge-focused PausedThis study followed children and young adults with genetic liver diseases that cause bile buildup. The goal was to track how these diseases progress over time, including the need for liver transplants or other complications. No treatments were tested; the aim was simply to learn …
Sponsor: Arbor Research Collaborative for Health • Aim: Knowledge-focused
Last updated Jun 27, 2026 13:02 UTC