Any primary immunodeficiency disease in which the cause of the disease is a mutation in the BCL11B gene.
Comprehensive, easy-to-understand information about this condition
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B cell deficiency
MONDO:0002211
complement deficiency
MONDO:0003832
phagocyte bactericidal dysfunction
MONDO:0005910
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency
MONDO:0007064
MHC class II deficiency
MONDO:0008855
trichohepatoenteric syndrome
MONDO:0009105