X-linked severe congenital neutropenia

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Summary

Literature (0)

DOID:0112128 - X-linked severe congenital neutropenia

Disease Ontology Definition:A severe congenital neutropenia that has_material_basis_in hemizygous activating mutation in WAS on chromosome Xp11.23.

Synonyms: SCNX, XLN,

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

OMIM:

MIM:300299 - neutropenia, severe congenital, x-linked; scnx

MIM:300299 - neutropenia, severe congenital, x-linked; scnx

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

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

Parent(s): severe congenital neutropenia (is_a)