agammaglobulinemia 3

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Summary

Literature (0)

DOID:0081137 - agammaglobulinemia 3

Disease Ontology Definition:An agammaglobulinemia that has_material_basis_in homozygous mutation in the CD79A gene on chromosome 19q13.2.

Synonyms:

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

: cd79a

MIM:

MIM:613501 - AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE; AGM3

MIM:613501 - AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE; AGM3

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

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

Parent(s): agammaglobulinemia (is_a), autosomal recessive disease (is_a)