A immunodeficiency disorder caused by loss of function mutation in NIK (MAP3K14).
Comprehensive, easy-to-understand information about this condition
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TCR-alpha-beta-positive T-cell deficiency
MONDO:0014160
non-severe combined immunodeficiency due to COPG1 deficiency
MONDO:0800136
HELIOS deficiency
MONDO:0800139
ITPKB deficiency
MONDO:0800140
MAN2B2 deficiency
MONDO:0800141
non-severe combined immunodeficiency due to polymerase delta deficiency
MONDO:0800145