NEUTROPENIA, SEVERE CONGENITAL, 7, AUTOSOMAL RECESSIVE; SCN7

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Summary

Literature (0)

MIM:617014 - NEUTROPENIA, SEVERE CONGENITAL, 7, AUTOSOMAL RECESSIVE; SCN7

Xenbase Genes: csf3r

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014865 - autosomal recessive severe congenital neutropenia due to CSF3R deficiency

MONDO:0014865 - autosomal recessive severe congenital neutropenia due to CSF3R deficiency

Disease Ontology (DO):

DOID:0112129 - severe congenital neutropenia 7

DOID:0112129 - severe congenital neutropenia 7