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Agammaglobulinemia 8B

Disease ID: disease_node_17351

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DbxrefMIM:619824
SubclassofDOID_2583, DOID_0050737
Data SourceDOID
Doid Labelagammaglobulinemia 8B
Doid DescriptionAn agammaglobulinemia that is characterized by onset of recurrent infections in early childhood and that has_material_basis_in homozygous loss-of-function mutation in the TCF3 gene on chromosome 19p13.
Existence Starts DuringHP_0011463
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_17351
Doid IdDOID_0081143
LabelAgammaglobulinemia 8B