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Echinobase
Summary Literature (0)
DOID:0060027 - agammaglobulinemia 4

Disease Ontology Definition:An agammaglobulinemia that has_material_basis_in a mutation a homozygous mutation in the BLNK gene on chromosome 10q23.2.

Synonyms: BLNK deficiency, B cell linker protein deficiency, B-cell linker protein deficiency

Echinobase Genes :


MIM:
MIM:613502 - agammaglobulinemia 4, autosomal recessive; agm4

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)