agammaglobulinemia 8A

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Summary

Literature (0)

DOID:0081140 - agammaglobulinemia 8A

Disease Ontology Definition:An agammaglobulinemia that has_material_basis_in heterozygous dominant-negative mutation in the TCF3 gene on chromosome 19p13.

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

: tcf3

MIM:

MIM:616941 - AGAMMAGLOBULINEMIA 8A, AUTOSOMAL DOMINANT; AGM8A

MIM:616941 - AGAMMAGLOBULINEMIA 8A, AUTOSOMAL DOMINANT; AGM8A

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 dominant disease (is_a)