immunodeficiency 107 Disease Ontology Browser

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immunodeficiency 107 (DOID:0061076)
Alliance: disease page
Synonyms: immunodeficiency 107 with susceptibility to invasive Staphylococcus aureus infection
Alt IDs: OMIM:619986
Definition: A primary immunodeficiency disease that is characterized by the development of invasive and severe life-threatening infections with S. aureus affecting the skin and/or lungs and that has_material_basis_in heterozygous mutation in the OTULIN gene on chromosome 5p15.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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