inlet ventricular septal defect Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description .A ventricular septal defect that involves the inlet of the right ventricular septum immediately inferior to the AV valve apparatus. (Human Phenotype Ontology, HP_0011622)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011622
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Genes

1 genes associated with the inlet ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GJA1 gap junction protein, alpha 1, 43kDa