CD79B, CD79b molecule, 974

N. diseases: 104; N. variants: 6
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1832241
Disease: Agammaglobulinemia, non-Bruton type
Agammaglobulinemia, non-Bruton type
0.300 GermlineCausalMutation disease ORPHANET Cutting edge: a hypomorphic mutation in Igbeta (CD79b) in a patient with immunodeficiency and a leaky defect in B cell development. 17675462 2007
CUI: C1832241
Disease: Agammaglobulinemia, non-Bruton type
Agammaglobulinemia, non-Bruton type
0.300 GermlineCausalMutation disease ORPHANET Mutations of the Igbeta gene cause agammaglobulinemia in man. 17709424 2007