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Summary Literature (0)
OMIM:300299 - NEUTROPENIA, SEVERE CONGENITAL, X-LINKED; SCNX


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

In Mondo Disease Ontology:
MONDO:0010294 - X-linked severe congenital neutropenia

Human Disease Resources: OMIM

Xenbase Genes: was