Term Name: immunodeficiency 65
Synonyms: IMD65, immunodeficiency 65, susceptibility to viral infections
Definition: A primary immunodeficiency disease characterized by onset in early infancy of recurrent and severe viral infections, impaired cellular type I interferon response, and poor outcomes after vaccination with live attenuated vaccines that has_material_basis_in homozygous or compound heterozygous mutation in the IRF9 gene on chromosome 14q12.
Ontology: Human Disease [DOID:0111978]   ( DOID:0111978 )

Relationships
is a type of: autosomal recessive disease primary immunodeficiency disease