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Disease Ontology Browser
autosomal dominant severe congenital neutropenia (DOID:0112130)
Alliance: disease page
Alt IDs: ORDO:486
Definition: A severe congenital neutropenia that has_material_basis_in heterozygous mutation of an autosomal gene.

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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Send questions and comments to User Support. 		last database update
04/30/2024
MGI 6.23 		The Jackson Laboratory