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Disease Ontology Browser
immunoglobulin alpha deficiency (DOID:0060025)
Alliance: disease page
Synonyms: gamma-A-globulin deficiency; IgA deficiency
Alt IDs: OMIM:137100, OMIM:269650, OMIM:609529, MESH:D017098, ORDO:69127, UMLS_CUI:C0162538
Definition: A B cell deficiency that is an autosomal recessive disorder that has_material_basis_in mutation in the IgA (CD79 alpha) antigen receptor.


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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last database update
11/10/2020
MGI 6.16
The Jackson Laboratory