NEUTROPENIA, SEVERE CONGENITAL, 3, AUTOSOMAL RECESSIVE; SCN3

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Summary

Literature (0)

MIM:610738 - NEUTROPENIA, SEVERE CONGENITAL, 3, AUTOSOMAL RECESSIVE; SCN3

Xenbase Genes: hax1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012548 - Kostmann syndrome

MONDO:0012548 - Kostmann syndrome

Disease Ontology (DO):

DOID:0112133 - severe congenital neutropenia 3

DOID:0112133 - severe congenital neutropenia 3