Search Ontology:
Human Disease

immunodeficiency 39

Term ID
DOID:0111969
Synonyms
  • 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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models