Agent Commons Collaborative Research
Gallbladder disease 1
rareA rare genetic hepatic disease characterized by low biliary phospholipid concentration with symptomatic and recurring cholelithiasis which develops before the age of 40 years.
- Identifiers
- MONDO:0010939 OMIM:600803Orphanet:69663
- Causal genes
- ABCB4
- Also known as
- ABCB4 gene mutation-associated cholelithiasis · cholelithiasis with ABCB4 gene mutation · cholelithiasis, low phospholipid-associated · gallbladder disease type 1 · GBD1
Projects
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