Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Specific granule deficiency 1

MONDO:0044207

Any 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

1 clinical trial for this condition and its sub-types, 0 tagged with Specific granule deficiency 1 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by