NEUTROPENIA, SEVERE CONGENITAL, 2, AUTOSOMAL DOMINANT; SCN2

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Summary

Literature (0)

MIM:613107 - NEUTROPENIA, SEVERE CONGENITAL, 2, AUTOSOMAL DOMINANT; SCN2

Xenbase Genes: gfi1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0008742 - autosomal dominant severe congenital neutropenia
MONDO:0013139 - neutropenia, severe congenital, 2, autosomal dominant

MONDO:0008742 - autosomal dominant severe congenital neutropenia

MONDO:0013139 - neutropenia, severe congenital, 2, autosomal dominant

Disease Ontology (DO):

DOID:0112131 - severe congenital neutropenia 2

DOID:0112131 - severe congenital neutropenia 2