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| Term | agammaglobulinemia 2 | ID (Ontology) | DOID:0081135 (Human Disease) |
| Definition | An agammaglobulinemia that has_material_basis_in homozygous or compound heterozygous mutation in the immunoglobulin lambda-like-1 gene (IGLL1) on chromosome 22q11. | ||
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autosomal genetic disease |__autosomal recessive disease__ B cell deficiency | |__agammaglobulinemia___________| agammaglobulinemia 2 |
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| Is a |
autosomal recessive disease agammaglobulinemia |
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| MIM:613500 | |||