Arterial calcification, generalized, of infancy, 2
MONDO:0013768Any 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, 2, arterial calcification, generalized, of infancy, type 2, GACI2
3 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsBroader categories
-
Can medical records unlock the secrets of rare calcification diseases?
Knowledge-focused CompletedThis study looks back at medical records of people with two rare genetic conditions—ENPP1 deficiency and the early-onset form of ABCC6 deficiency—to map how these diseases progress over time. By collecting information on symptoms, imaging, and growth, researchers hope to better u…
Sponsor: Inozyme Pharma • Aim: Knowledge-focused
Last updated Aug 06, 2026 00:00 UTC
-
Rare disease detectives: new study maps how two genetic conditions unfold in children
Knowledge-focused CompletedThis study follows children aged 2 to 18 with confirmed ENPP1 deficiency or early-onset ABCC6 deficiency to understand how these rare diseases progress. Researchers will measure blood markers, check for calcification in arteries and organs, and track bone health and movement over…
Sponsor: Inozyme Pharma • Aim: Knowledge-focused
Last updated Jul 08, 2026 00:00 UTC