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Echinobase
Summary Literature (0)
DOID:2583 - agammaglobulinemia


Disease Ontology Definition:A B cell deficiency that is caused by a reduction in all types of gamma globulins.

Synonyms: IGHM, hypogammaglobulinemia, mu heavy chain deficiency,

Echinobase Genes : LOC588766


OMIM:
MIM:601495 - agammaglobulinemia 1, autosomal recessive; agm1
MIM:613501 - agammaglobulinemia 3, autosomal recessive; agm3
MIM:613502 - agammaglobulinemia 4, autosomal recessive; agm4
MIM:615214 - agammaglobulinemia 7, autosomal recessive; agm7

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): B cell deficiency (is_a)