Gallbladder disease 1

A rare genetic hepatic disease characterized by low biliary phospholipid concentration with symptomatic and recurring cholelithiasis which develops before the age of 40 years.

Also known as: ABCB4 gene mutation-associated cholelithiasis, GBD1, LPAC, cholelithiasis with ABCB4 gene mutation, cholelithiasis, low phospholipid-associated, gallbladder disease 1, gallbladder disease type 1, low phospholipid associated cholelithiasis

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