Disease #02316 (GBD1;LPAC (gallbladder disease, type 1 (GBD-1, cholelithiasis, low-phospholipid associated (LPAC))), OMIM:600803)

Official abbreviation GBD1;LPAC
Name gallbladder disease, type 1 (GBD-1, cholelithiasis, low-phospholipid associated (LPAC))
OMIM ID 600803
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 3
Associated with 1 gene ABCB4
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00181085 Pat4 PubMed: Huynh 2019 - F no - - - - - Ursodeoxycholic acid treatment GBD1;LPAC Multiple episodes of epigastric pain after meals, vomiting, nausea. Ultrasound: multiple intrahepatic microlithiasis, cholecystectomy, ursodeoxycholic acid treatment. ABCC4 ABCB4 1 1 Minh Tuan Huynh
00181086 Pat5 PubMed: Huynh 2019 - F - - - - - - ursodeoxycholic acid treatment GBD1;LPAC symptomatic gallstone disease, cholecystectomy at the age of 24, epigastric pain radiating to the right hypochondrium, increased after meals. Increased level of transaminases and GGT. Ultrasound: comet-tails, moderate dilatation of intrahepatic bile ducts, ursodeoxycholic acid treatment ABCB4 ABCB4 1 1 Minh Tuan Huynh
00226258 - - - M - Turkey - - - - - GBD1;LPAC - ABCB4 ABCB4 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00416010 Pat3 PubMed: Huynh 2019 - - - - - - - - - GBD1;LPAC - ABCB4 ABCB4 2 1 Johan den Dunnen
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