Neutropenia, severe congenital, 2, autosomal dominant

rare

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

Identifiers: MONDO:0013139 OMIM:613107
Causal genes: GFI1
Part of: Autosomal dominant severe congenital neutropenia
Also known as: autosomal dominant severe congenital neutropenia caused by mutation in GFI1 · GFI1 autosomal dominant severe congenital neutropenia · neutropenia, severe congenital 2, autosomal dominant · SCN2

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