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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 - scleral endothelium

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