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Summary Literature (0)
MIM:618752 - NEUTROPENIA, SEVERE CONGENITAL, 8, AUTOSOMAL DOMINANT; SCN8

Xenbase Genes:

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0032899 - neutropenia, severe congenital, 8, autosomal dominant

Disease Ontology (DO):
DOID:0112135 - severe congenital neutropenia 8