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

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

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

: was

MIM:

MIM:300299 - NEUTROPENIA, SEVERE CONGENITAL, X-LINKED; SCNX

MIM:300299 - NEUTROPENIA, SEVERE CONGENITAL, X-LINKED; SCNX

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

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

Parent(s): severe congenital neutropenia (is_a), X-linked recessive disease (is_a)