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HELIOS deficiency
MONDO:0800139A non-severe combined immunodeficiency caused by a loss-of-function variation in the IKZF2 gene that is characterized by recurrent upper respiratory infections, thrush and mucosal ulcers, and chronic lymphadenopathy.
15 clinical trials for this condition and its sub-types.
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Disease
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Hereditary disease
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Immune system disorder
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Immunodeficiency disease
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Human disease
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Combined immunodeficiency
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Disease of genetic or genomic mechanism
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Disease by body system or component
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Disease by etiologic mechanism
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Non-SCID combined immunodeficiency
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