Severe Congenital Neutropenia Type 2, Autosomal Dominant

**Semantic type:** Disease or Syndrome

**Definition:** Severe congenital neutropenia inherited in an autosomal dominant pattern and caused by mutation(s) in the GFI1 gene, encoding zinc finger protein Gfi-1.

**Synonyms:** - Neutropenia, Severe Congenital, 2, Autosomal Dominant - SCN 2-Autosomal Dominant - SCN2