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Metadata
ID	DOID:0111969
Name	immunodeficiency 39
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/
Xrefs	MIM:616345
Synonyms	IMD39 [EXACT]
Parent Relationships	is_a autosomal dominant disease is_a primary immunodeficiency disease
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance