has material basis in disease has location autosomal dominant disease immunodeficiency 107 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. DOID:0061076 disease_ontology MIM:619986 immunodeficiency 107 with susceptibility to invasive Staphylococcus aureus infection primary immunodeficiency disease lung disease autosomal dominant inheritance zone of skin lung