MONDO_0013768 (arterial calcification, generalized, of infancy, 2) is any arterial calcification of infancy in which the cause of the disease is a mutation in the ABCC6 gene. Also known as: ABCC6 arterial calcification of infancy, arterial calcification of infancy caused by mutation in ABCC6, arterial calcification, generalized, of infancy, type 2.