Specific granule deficiency 1
MONDO:0044207Any specific granule deficiency in which the cause of the disease is a mutation in the CEBPE gene.
Also known as: specific granule deficiency, CEBPE specific granule deficiency, specific granule deficiency 1, specific granule deficiency caused by mutation in CEBPE, SGD1, lactoferrin-deficient neutrophils, neutrophil lactoferrin deficiency
43 clinical trials for this condition and its sub-types.
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