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MAN2B2 deficiency
MONDO:0800141Any non-severe combined immunodeficiency in which the cause of the disease is variation in the MAN2B2 gene.
15 clinical trials for this condition and its sub-types.
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Disease
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Hereditary disease
(172)
Immune system disorder
(140)
Immunodeficiency disease
(48)
Human disease
(14)
Combined immunodeficiency
(3)
Disease of genetic or genomic mechanism
(2)
Disease by body system or component
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Disease by etiologic mechanism
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Non-SCID combined immunodeficiency
(0)