pulmonary venoocclusive disease Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_5453)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006518
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Genes

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

Symbol Name
BMPR2 bone morphogenetic protein receptor, type II (serine/threonine kinase)