Neutropenia, severe congenital, 2, autosomal dominant

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

42 clinical trials for this condition and its sub-types.