NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE; SCN6

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Summary

Literature (0)

MIM:616022 - NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE; SCN6

Xenbase Genes: jagn1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014456 - autosomal recessive severe congenital neutropenia due to JAGN1 deficiency

MONDO:0014456 - autosomal recessive severe congenital neutropenia due to JAGN1 deficiency

Disease Ontology (DO):

DOID:0112134 - severe congenital neutropenia 6

DOID:0112134 - severe congenital neutropenia 6