Familial hypercholanemia

Disease Export to PDF
Name:
Familial hypercholanemia
Description:
Familial hypercholanemia is 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.
ORPHAcode:
238475
Synonyms:
Hereditary hypercholanemia
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14