Arterial calcification of infancy Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
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1 genes/proteins associated with the disease Arterial calcification of infancy from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1 2.88009