|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A congenital defect with aplasia (absence) of one of the right or left pulmonary artery. (Human Phenotype Ontology, HP_0004960)|
|Downloads & Tools|
1 genes associated with the absent pulmonary artery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|CRTAP||cartilage associated protein|