Omenn syndrome
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Revision as of 21:15, 8 March 2020 by Aidan (talk | contribs) (Created page with "* Syndrome of erythroderma, desquamation, organomegaly with eosinophilia, and hypomorphic severe combined immunodeficiency * Caused by a number of mutations that commonly...")
- Syndrome of erythroderma, desquamation, organomegaly with eosinophilia, and hypomorphic severe combined immunodeficiency
- Caused by a number of mutations that commonly involve RAG1 or RAG2
