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| Term | recombinase activating gene 1 deficiency | ID (Ontology) | DOID:0060011 (Human Disease) |
| Definition | A severe combined immunodeficiency that is the result of a mutation on Chromosome 6 RAG1 gene involving genetic rearrangement of both the T- and B-lymphocyte receptor genes. | ||
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combined immunodeficiency |__severe combined immunodeficiency |__recombinase activating gene 1 deficiency |
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| Is a | severe combined immunodeficiency | ||
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