FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
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Term agammaglobulinemia 10 ID (Ontology) DOID:0081142 (Human Disease)
Definition An agammaglobulinemia that is characterized by early-childhood onset of recurrent viral and bacterial infections affecting various organ systems, particularly the sinopulmonary system, and that has_material_basis_in heterozygous mutation in the SPI1 gene on chromosome 11p11.
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 agammaglobulinemia 10       1
 for disease ribbon | agammaglobulinemia 10       1
 model of | agammaglobulinemia 10       1
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autosomal genetic disease
 |__autosomal dominant disease__
B cell deficiency               |
 |__agammaglobulinemia__________|
                                agammaglobulinemia 10  1 rec.
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Is a autosomal dominant disease
agammaglobulinemia
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MIM:619707