|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A disorder of large arteries, in particular the aorta, characterized by an accumulation of basophilic ground substance in the media with cyst-like lesions associated with degenerative changes of collagen, elastin and the vascular smooth muscle cells. (Human Phenotype Ontology, HP_0012180)|
|Downloads & Tools|
1 genes associated with the cystic medial necrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|MYH11||myosin, heavy chain 11, smooth muscle|