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Summary Literature (0)
MIM:613107 - NEUTROPENIA, SEVERE CONGENITAL, 2, AUTOSOMAL DOMINANT; SCN2

Xenbase Genes: gfi1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008742 - autosomal dominant severe congenital neutropenia
MONDO:0013139 - ligament of liver

Disease Ontology (DO):
DOID:0112131 - severe congenital neutropenia 2