Immunodeficiency 47

Any primary immunodeficiency disease in which the cause of the disease is a mutation in the ATP6AP1 gene.

Also known as: ATP6AP1 primary immunodeficiency disease, IMD47, immunodeficiency 47, immunodeficiency 47, X-linked recessive, immunodeficiency 47; IMD47, immunodeficiency type 47, primary immunodeficiency disease caused by mutation in ATP6AP1, immunodeficiency and hepatopathy with or without neurologic features

41 clinical trials for this condition and its sub-types, 0 tagged with Immunodeficiency 47 itself.