pulmonary artery atresia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A congenital anomaly with e narrowing or complete absence of the opening between the right ventricle and the pulmonary artery. (Human Phenotype Ontology, HP_0004935)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004935
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5 genes associated with the pulmonary artery atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CRELD1 cysteine-rich with EGF-like domains 1
FADD Fas (TNFRSF6)-associated via death domain
GDF1 growth differentiation factor 1
NKX2-5 NK2 homeobox 5
STRA6 stimulated by retinoic acid 6