arterial intimal fibrosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Formation of excess fibrous connective tissue in the tunica intima (innermost layer) of arteries. (Human Phenotype Ontology, HP_0011353)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011353
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Genes

1 genes associated with the arterial intimal fibrosis 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)