X-linked severe congenital neutropenia Disease Ontology Browser

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Disease Ontology Browser

X-linked severe congenital neutropenia (DOID:0112128)
Alliance: disease page
Synonyms: SCNX; XLN
Alt IDs: OMIM:300299, MESH:C564539, NCI:C176818, ORDO:86788, UMLS_CUI:C1845987
Definition: A severe congenital neutropenia that has_material_basis_in hemizygous activating mutation in WAS on chromosome Xp11.23.

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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