Non-severe combined immunodeficiency due to COPG1 deficiency
MONDO:0800136Any non-severe combined immunodeficiency caused by a deficiency in the COPG1 gene.
15 clinical trials for this condition and its sub-types.
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Disease
(618)
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
(0)
Disease by etiologic mechanism
(0)
Non-SCID combined immunodeficiency
(0)