femoral hernia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A hernia which occurs just below the inguinal ligament, where abdominal contents pass through a naturally occurring weakness called the femoral canal. (Human Phenotype Ontology, HP_0100541)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100541
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Genes

1 genes associated with the femoral hernia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
TBX1 T-box 1