Search Ontology:
Human Disease
immunodeficiency 39
- Term ID
- DOID:0111969
- Synonyms
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- IMD39
- Definition
- A primary immunodeficiency disease characterized by impaired interferon I and III production in response to influenza virus infection that has_material_basis_in homozygous or compond heterozygous mutation in the IRF7 gene on chromosome 11p15.5. https://pubmed.ncbi.nlm.nih.gov/25814066/
- References
- Ontology
- Human Disease ( DOID:0111969 )
- is a type of
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Genes Involved
Zebrafish Models