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Disease Ontology Browser
severe congenital neutropenia (DOID:0050590)
Alliance: disease page
Alt IDs: OMIM:202700, OMIM:300299, OMIM:610738, OMIM:612541, OMIM:613107, OMIM:615285, OMIM:616022, ICD10CM:D70, ORDO:486, ORDO:86788
Definition: A neutropenia characterized by a maturation arrest of granulopoiesis at the level or promyelocytes and early onset of severe bacterial infections.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory