|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Formation of excess fibrous connective tissue in the tunica intima (innermost layer) of arteries in the pulmonary circulation. (Human Phenotype Ontology, HP_0005312)|
|Downloads & Tools|
1 genes associated with the pulmonary aterial intimal fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|BMPR2||bone morphogenetic protein receptor, type II (serine/threonine kinase)|