Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:612541 - NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4

Xenbase Genes: g6pc3, g6pc3.2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012930 - autosomal recessive severe congenital neutropenia due to G6PC3 deficiency

Disease Ontology (DO):
DOID:0050590 - severe congenital neutropenia
DOID:0112136 - severe congenital neutropenia 4