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Omenn Syndrome — Gene Therapy & Clinical Trials | FollowGene
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Omenn Syndrome
Omenn Syndrome
Prevalence:
1/500000
immunologic
Official
·
OMIM:603554
Official
·
ORPHA39041
Atypical SCID and erythroderma due to RAG1/RAG2 gene mutations.
Associated Genes
RAG1
Recombination Activating 1
Chromosome 11
Autosomal Recessive
RAG2
Recombination Activating 2
Chromosome 11
Autosomal Recessive