|OBO ID: DOID:0060010|
|Term Name:||Omenn syndrome||Search Ontology:|
|Definition:||A severe combined immunodeficiency that has_material_basis in the RAG1 and RAG2 genes on chromosome 11p and the Artemis gene on chromosome 10p. It is characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly. (3)|
|Ontology:||Human Disease (DOID:0060010)|
|is a type of:||
OTHER Omenn syndrome PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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