immunoglobulin alpha deficiency

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Echinobase

Summary

Literature (0)

DOID:0060025 - immunoglobulin alpha deficiency

Disease Ontology Definition:A B cell deficiency that is an autosomal recessive disorder that has_material_basis_in mutation in the IgA (CD79 alpha) antigen receptor.

Synonyms: IgA deficiency, gamma-A-globulin deficiency,

Echinobase 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

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

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

Parent(s): B cell deficiency (is_a), autosomal recessive disease (is_a)