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| Term | agammaglobulinemia 5 | ID (Ontology) | DOID:0080588 (Human Disease) |
| Definition | An agammaglobulinemia that has_material_basis_in heterozygous mutation in the LRRC8A gene on chromosome 9q34. | ||
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autosomal genetic disease |__autosomal dominant disease__ B cell deficiency | |__agammaglobulinemia__________| agammaglobulinemia 5 |
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| Is a |
autosomal dominant disease agammaglobulinemia |
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| MIM:613506 | |||