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

In OMIM:

OMIM:601495 - AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE; AGM1

OMIM:612692 - AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE; AGM6

OMIM:613500 - AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE; AGM2

OMIM:613501 - AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE; AGM3

OMIM:613502 - AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE; AGM4

OMIM:615214 - AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE; AGM7

In Mondo Disease Ontology:

MONDO:0015977 - agammaglobulinemia

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : prkcd, ms4a1, cd19, cd79a, cd81, blnk, lrba, nfkb2, nfkb1, lrrc8a, pik3r1, btk, cd79b, tnfsf12

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