Immunodeficiency 37

MONDO:0014491

Any primary immunodeficiency disease in which the cause of the disease is a mutation in the BCL10 gene.

Also known as: BCL10 primary immunodeficiency disease, combined immunodeficiency due to BCL10 deficiency, immunodeficiency 37, immunodeficiency type 37, primary immunodeficiency disease caused by mutation in BCL10, IMD37

41 clinical trials for this condition and its sub-types, 0 tagged with Immunodeficiency 37 itself.

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Part of

↑ Hereditary disease (18230) ↑ Inborn error of immunity (344)

Sub-types of Immunodeficiency 37

Combined immunodeficiency with low Ig due to BCL10 deficiency 0 trials

Including sub-types (41) Tagged with Immunodeficiency 37 (0)

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