Hypercholanemia, familial 1

MONDO:0031446

A very rare genetic disorder characterized clinically by elevated serum bile acid concentrations, itching, and fat malabsorption reported in patients of Old Order Amish descent.

Also known as: hereditary hypercholanemia, FHCA1

1 clinical trial for this condition and its sub-types, 0 tagged with Hypercholanemia, familial 1 itself.

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Including sub-types (1) Tagged with Hypercholanemia, familial 1 (0)

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