Omenn syndrome (Q2214419)

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Human disease
  • combined immunodeficiency with hypereosinophilia
  • Severe Combined Immunodeficiency With Hypereosinophilia
  • Reticuloendotheliosis, Familial, With Eosinophilia
  • OMENN SYNDROME
  • Reticuloendotheliosis familial with eosinophilia
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Language Label Description Also known as
English
Omenn syndrome
Human disease
  • combined immunodeficiency with hypereosinophilia
  • Severe Combined Immunodeficiency With Hypereosinophilia
  • Reticuloendotheliosis, Familial, With Eosinophilia
  • OMENN SYNDROME
  • Reticuloendotheliosis familial with eosinophilia

Statements

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Omenn syndrome
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Identifiers

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