Search Ontology:
Human Disease

immunodeficiency 65

Term ID
DOID:0111978
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. (2)
References
Ontology
Human Disease   ( DOID:0111978 )
Relationships
is a type of
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Genes Involved
Zebrafish Models