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| Term | common variable immunodeficiency 6 | ID (Ontology) | DOID:0081149 (Human Disease) |
| Definition | A common variable immunodeficiency that has_material_basis_in homozygous mutation in the CD81 gene on chromosome 11p. | ||
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| DO.org | |||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal recessive disease__ agammaglobulinemia___________| common variable immunodeficiency |__common variable immunodeficiency 6 4 rec. |
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| Is a | common variable immunodeficiency | ||
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| MIM:613496 | |||