Neutropenia, Severe Congenital, 9, Autosomal Dominant (SCN9)

Neutropenia, Severe Congenital, 9, Autosomal Dominant, also known as scn9, is related to clpb deficiency and 3-methylglutaconic aciduria, type viia. An important gene associated with Neutropenia, Severe Congenital, 9, Autosomal Dominant is CLPB (ClpB Family Mitochondrial Disaggregase). Affiliated tissues include bone marrow and myeloid, and related phenotypes are myeloid maturation arrest and seizure