Any autosomal dominant severe congenital neutropenia in which the cause of the disease is a mutation in the GFI1 gene. The disease is Monarch Disease Ontology entry MONDO_0013139 (neutropenia, severe congenital, 2, autosomal dominant). 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.