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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 IRF7 on chromosome 11p15.5.
https://pubmed.ncbi.nlm.nih.gov/25814066/
Xrefs

OMIM:616345

Synonyms

IMD39 [EXACT]

Parent Relationships

is_a primary immunodeficiency disease

is_a autosomal dominant disease

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