absent pulmonary artery Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A congenital defect with aplasia (absence) of one of the right or left pulmonary artery. (Human Phenotype Ontology, HP_0004960)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004960
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Genes

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

Symbol Name
CRTAP cartilage associated protein