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Arterial calcification, generalized, of infancy, 2

MONDO:0013768

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, 2, arterial calcification, generalized, of infancy, type 2, GACI2

3 clinical trials for this condition and its sub-types.

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Broader categories

Cardiovascular disorder (1093) Disease (717) Hereditary disease (188) Vascular disorder (138) Human disease (15) Arterial calcification of infancy (7) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0)
Not yet finished but already full! 1 Completed 2
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  • New registry aims to unlock secrets of rare genetic diseases

    Knowledge-focused Ongoing

    This observational registry is collecting information from up to 1,000 people with ENPP1 deficiency or infantile-onset ABCC6 deficiency. The goal is to understand how these rare diseases progress over time by tracking genetic, physical, and quality-of-life changes during routine …

    Sponsor: Inozyme Pharma • Aim: Knowledge-focused

    Last updated Aug 30, 2026 00:00 UTC

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