|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A vascular disease that is characterized by generalized calcification of the arterial internal elastic lamina, leading to rupture of the lamina and occlusive changes in the tunica intima with stenosis and decreased elasticity of the vessel wall. (Human Disease Ontology, DOID_0050644)|
|Downloads & Tools|
1 genes/proteins associated with the disease Arterial calcification of infancy from the curated CTD Gene-Disease Associations dataset.
|ENPP1||ectonucleotide pyrophosphatase/phosphodiesterase 1||2.88009|