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Summary Literature (0)
MIM:202700 - NEUTROPENIA, SEVERE CONGENITAL, 1, AUTOSOMAL DOMINANT; SCN1

Xenbase Genes: gfi1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0042490 - neutropenia, severe congenital, 1, autosomal dominant

Disease Ontology (DO):
DOID:0050590 - severe congenital neutropenia
DOID:0080625 - severe congenital neutropenia 1