absent gallbladder Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A developmental defect in which the gallbladder fails to form. (Human Phenotype Ontology, HP_0011467)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011467
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1 genes associated with the absent gallbladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
RFX6 regulatory factor X, 6