Immunodeficiency 81
MONDO:0030302A human immunodeficiency characterized by early-onset life-threatening infections, combined T and B cell immunodeficiency, severe neutrophil defects, and impaired platelet aggregation, caused by a variation in the SLP76 gene.
Also known as: IMD81, T-B+ severe combined immunodeficiency due to SLP76 deficiency, immunodeficiency 81
0 clinical trials for this condition and its sub-types, 0 tagged with Immunodeficiency 81 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Part of
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.