A combined immunodeficiency in which the cause of the disease is a variation in the NFATC1 gene.
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ataxia telangiectasia
MONDO:0008840
combined immunodeficiency due to ZAP70 deficiency
MONDO:0010023
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia
MONDO:0010455
combined immunodeficiency due to moesin deficiency
MONDO:0010514
Wiskott-Aldrich syndrome
MONDO:0010518
MHC class I deficiency
MONDO:0011476