X-linked Mendelian susceptibility to mycobacterial diseases
MONDO:0017905A rare group of immunodeficiencies due to specific mutations in the inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma (IKBKG) or the cytochrome b-245, beta polypeptide (CYBB) genes. They are characterized by mycobacterial infections, occurring in males.
Also known as: X-linked MSMD, mendelian susceptibility to mycobacterial diseases, X-linked
0 clinical trials for this condition and its sub-types, 0 tagged with X-linked Mendelian susceptibility to mycobacterial diseases itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of X-linked Mendelian susceptibility to mycobacterial diseases
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.