agammaglobulinemia 2

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Summary

Literature (0)

DOID:0081135 - agammaglobulinemia 2

Disease Ontology Definition:An agammaglobulinemia that has_material_basis_in homozygous or compound heterozygous mutation in the immunoglobulin lambda-like-1 gene (IGLL1) on chromosome 22q11.

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

MIM:

MIM:613500 - AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE; AGM2

MIM:613500 - AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE; AGM2

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)