has material basis in germline mutation in ABCB4 cholecystitis gallbladder disease 1 https://github.com/monarch-initiative/mondo/issues/8630 https://www.malacards.org/card/gallbladder_disease_1 LPAC icd11.foundation:1261516421 OMIM:600803 SCTID:715577009 Orphanet:69663 GARD:0016683 gallbladder disease type 1 MedDRA:10068936 MEDGEN:760527 GBD1 MONDO:0010939 A rare genetic hepatic disease characterized by low biliary phospholipid concentration with symptomatic and recurring cholelithiasis which develops before the age of 40 years. gallbladder disease 1 UMLS:C2609268 cholelithiasis, low phospholipid-associated cholelithiasis with ABCB4 gene mutation ABCB4 gene mutation-associated cholelithiasis low phospholipid associated cholelithiasis cholelithiasis hereditary gallbladder disorder