Cholestasis, progressive familial intrahepatic, 5

Any progressive familial intrahepatic cholestasis in which the cause of the disease is a mutation in the NR1H4 gene.

Also known as: NR1H4 deficiency, NR1H4 progressive familial intrahepatic cholestasis, PFIC5, cholestasis, progressive familial intrahepatic, 5, cholestasis, progressive familial intrahepatic, 5; PFIC5, cholestasis, progressive familial intrahepatic, type 5, progressive familial intrahepatic cholestasis caused by mutation in NR1H4

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