immunodeficiency 39

Summary

DOID:0111969 - immunodeficiency 39

Disease Ontology 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.

Synonyms: IMD39

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: irf7

MIM:

MIM:616345 - IMMUNODEFICIENCY 39; IMD39

MIM:616345 - IMMUNODEFICIENCY 39; IMD39

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), primary immunodeficiency disease (is_a)