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Omenn Syndrome

Omenn Syndrome [RAG2]: A severe form of immunodeficiency characterized by T-cell infiltration of skin, gut, liver, and spleen, leading to diffuse erythroderma, protracted diarrhea, failure to thrive, and hepatosplenomegaly.

For detailed information about this disease visit : National Institutes of Health (NIH) >

Carrier Frequency by Ethnicity >