Describes a rare group of immunodeficiencies due to specific mutations in the inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma (IKBKG) or the cytochrome b-245, beta polypeptide (CYBB) genes. The clinical manifestation is my
SNOMEDCT-BE (disorder) / 719814009
SNOMEDCT-BE (IKBKG) or the cytochrome b-245, beta polypeptide (CYBB) genes. The clinical manifestation is my / 719814009
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