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bn:01607077n
Noun Concept
Categories: Noninfectious immunodeficiency-related cutaneous conditions, Autosomal recessive disorders, Rare syndromes, Hepatology, Combined T and B–cell immunodeficiencies
EN
Omenn syndrome  combined immunodeficiency with hypereosinophilia  Omenn's syndrome  Reticuloendotheliosis, Familial, With Eosinophilia  Reticuloendotheliosis familial with eosinophilia
EN
Omenn syndrome is an autosomal recessive severe combined immunodeficiency. Wikipedia
Definitions
Relations
Sources
EN
Omenn syndrome is an autosomal recessive severe combined immunodeficiency. Wikipedia
Human disease Wikidata
IS A
rare disease
severe combined immunodeficiency
GENETIC ASSOCIATION
DCLRE1C
RAG1
RAG2
HEALTH SPECIALTY
hematology
SYMPTOMS
diarrhea
hepatosplenomegaly
Wikipedia
EN
Omenn syndrome
Wikidata
EN
Omenn syndrome
Wikipedia Redirections
EN
Omenn's syndrome
Wikidata Alias
EN
combined immunodeficiency with hypereosinophilia, OMENN SYNDROME, Reticuloendotheliosis, Familial, With Eosinophilia, Reticuloendotheliosis familial with eosinophilia, Severe Combined Immunodeficiency With Hypereosinophilia

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