/neutropenia, severe congenital, 2, autosomal dominant
neutropenia, severe congenital, 2, autosomal dominant
Rare Disease
MONDO:0013139
Also Known As
GFI1 autosomal dominant severe congenital neutropeniaautosomal dominant severe congenital neutropenia caused by mutation in GFI1neutropenia, severe congenital 2, autosomal dominantneutropenia, severe congenital, 2, autosomal dominantSCN2
Definition
Any autosomal dominant severe congenital neutropenia in which the cause of the disease is a mutation in the GFI1 gene.
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