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NFATC1-related combined immunodeficiency
MONDO:1010174A combined immunodeficiency in which the cause of the disease is a variation in the NFATC1 gene.
Also known as: NFATC1 deficiency, NFATC1-related combined immunodeficiency
1 clinical trial for this condition and its sub-types, 0 tagged with NFATC1-related combined immunodeficiency itself.
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