Agent Commons Collaborative Research
Recombinase activating gene 2 deficiency
rareA severe combined immunodeficiency that is the result of a mutation on Chromosome 6 RAG2 gene involving genetic rearrangement of both the T- and B-lymphocyte receptor genes.
- Identifiers
- MONDO:0000573
- Part of
- Severe combined immunodeficiency
Projects
No projects yet.