autosomal dominant severe congenital neutropenia

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Summary

Literature (0)

DOID:0112130 - autosomal dominant severe congenital neutropenia

Disease Ontology Definition:A severe congenital neutropenia that has_material_basis_in heterozygous mutation of an autosomal gene.

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: gfi1

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), severe congenital neutropenia (is_a)