An immunodeficiency disease in which the cause of the disease is a variation in the TNFRSF9 gene.
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B cell deficiency
MONDO:0002211
T-cell immunodeficiency
MONDO:0003780
complement deficiency
MONDO:0003832
myalgic encephalomeyelitis/chronic fatigue syndrome
MONDO:0005404
hypoproteinemia, hypercatabolic
MONDO:0009434
X-linked lymphoproliferative syndrome
MONDO:0010627