Neutropenia, severe congenital, 2, autosomal dominant

MONDO:0013139

Any autosomal dominant severe congenital neutropenia in which the cause of the disease is a mutation in the GFI1 gene.

Also known as: GFI1 autosomal dominant severe congenital neutropenia, autosomal dominant severe congenital neutropenia caused by mutation in GFI1, neutropenia, severe congenital 2, autosomal dominant, neutropenia, severe congenital, 2, autosomal dominant, SCN2

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