Human genes for immunoglobulin alpha deficiency
Immunoglobulin alpha deficiency [DOID:0060025]
A B cell deficiency that is an autosomal recessive disorder that has_material_basis_in mutation in the IgA (CD79 alpha) antigen receptor.
Synonyms: immunoglobulin alpha deficiency, DOID:0060025, immunoglobulin alpha deficiencies, gamma-A-globulin deficiency, IgA deficiency ...
Linkouts: OMIM