Congenital liver fibrosis, PKHD1-related, horse

A developmental disorder of the biliary system caused by a congenital defect in the remodeling of the ductal plate at the level of the interlobular ducts, resulting in persistence of excessive abnormal embryonic bile duct structures, irregular portal veins, and progressive fibrosis of the portal tracts that occurs in horses due to a mutation in the PKHD1 gene.

Also known as: congenital hepatic fibrosis, horse, congenital liver fibrosis, horse

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