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Summary Literature (0)
DOID:0080625 - severe congenital neutropenia 1


Disease Ontology Definition:A severe congenital neutropenia that has_material_basis_in heterozygous mutation in the neutrophil elastase gene on chromosome 19p13.

Synonyms:

Xenbase Genes : 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)