TNFRSF9-related immunodeficiency

MONDO:0700308

An immunodeficiency disease in which the cause of the disease is a variation in the TNFRSF9 gene.

Also known as: 41BB deficiency, CD137 deficiency, TNFRSF9-related immunodeficiency

0 clinical trials for this condition and its sub-types, 0 tagged with TNFRSF9-related immunodeficiency itself.

Where it sits in the disease tree

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Sub-types of TNFRSF9-related immunodeficiency

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