Severe combined immunodeficiency due to IKK2 deficiency

MONDO:0014267

Severe combined immunodeficiency due to IKK2 deficiency is a rare, genetic form of primary immunodeficiency characterized by life-threatening bacterial, fungal and viral infections with the onset in infancy, and failure to thrive. Typically, hypogammaglobulinemia or agammaglobulinemia and normal levels of T and B cells are present.

Also known as: SCID due to IKK2 deficiency, immunodeficiency 15B, immunodeficiency type 15, IMD15, immunodeficiency 15

2 clinical trials for this condition and its sub-types, 0 tagged with Severe combined immunodeficiency due to IKK2 deficiency itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ T+ B+ severe combined immunodeficiency (0)

Including sub-types (2) Tagged with Severe combined immunodeficiency due to IKK2 deficiency (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.