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:300299 - NEUTROPENIA, SEVERE CONGENITAL, X-LINKED; SCNX

Xenbase Genes: was

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010294 - X-linked severe congenital neutropenia

Disease Ontology (DO):
DOID:0050590 - severe congenital neutropenia
DOID:0112128 - X-linked severe congenital neutropenia