severe congenital neutropenia 1 Disease Ontology Browser

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severe congenital neutropenia 1 (DOID:0080625)
Alliance: disease page
Alt IDs: OMIM:202700
Definition: A severe congenital neutropenia that has_material_basis_in heterozygous mutation in the neutrophil elastase gene on chromosome 19p13.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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