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Summary Literature (0)
MIM:615285 - NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE; SCN5

Xenbase Genes: vps45

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014118 - congenital neutropenia-myelofibrosis-nephromegaly syndrome

Disease Ontology (DO):
DOID:0050590 - severe congenital neutropenia
DOID:0112132 - severe congenital neutropenia 5