Immunodeficiency 39

Summary

A rare primary immunodeficiency with characteristics of a severe, potentially life-threatening course of influenza A infection with acute respiratory distress. Production of type I and III interferons in response to influenza virus is very low, while other immunological abnormalities are absent and no further unusual viral infections occur. [from SNOMEDCT_US]

Available tests

6 tests are in the database for this condition.

Clinical tests (6 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

IRF7
Also known as: IMD39, IRF-7, IRF-7H, IRF7A, IRF7B, IRF7C, IRF7H, IRF7
Summary: interferon regulatory factor 7

Imported from Human Phenotype Ontology (HPO)

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Abnormality of the immune system
- Immunodeficiency
  Immunodeficiency
  - MedGen UID: 7034
  - Concept ID: C0021051
  - Finding: Disease or Syndrome
  Abnormality of the immune system
  See: Feature record | Search on this feature
- Severe influenza infection
  Severe influenza infection
  - MedGen UID: 1814393
  - Concept ID: C5676829
  - Finding: Disease or Syndrome
  Abnormality of the immune system
  See: Feature record | Search on this feature

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Clinical resources

Molecular resources

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