Mondo Description Any arterial calcification of infancy in which the cause of the disease is a mutation in the ABCC6 gene.

Uniprot Description A severe autosomal recessive disorder characterized by calcification of the internal elastic lamina of muscular arteries and stenosis due to myointimal proliferation. The disorder is often fatal within the first 6 months of life because of myocardial ischemia resulting in refractory heart failure.