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bn:01607077n
Noun Concept
SYL
No term available
EN
Omenn syndrome is an autosomal recessive severe combined immunodeficiency. Wikipedia
Relations
Sources
IS A
EN
rare disease
EN
severe combined immunodeficiency
GENETIC ASSOCIATION
EN
DCLRE1C
EN
RAG1
EN
RAG2
HEALTH SPECIALTY
EN
hematology
SYMPTOMS
EN
diarrhea
EN
hepatosplenomegaly

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