aplasia/hypoplasia of the gallbladder Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the gallbladder. (Human Phenotype Ontology, HP_0011466)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011466
Similar Terms
Downloads & Tools

Genes

1 genes associated with the aplasia/hypoplasia of the gallbladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
RFX6 regulatory factor X, 6