Recombinase activating gene 1 deficiency

MONDO:0000572

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.

Also known as: recombinase activating gene 1 deficiency

2 clinical trials for this condition and its sub-types, 0 tagged with Recombinase activating gene 1 deficiency itself.

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↑ Severe combined immunodeficiency (37)

Including sub-types (2) Tagged with Recombinase activating gene 1 deficiency (0)

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