Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare primary immunodeficiency characterized by recurrent and/or invasive bacterial, viral, and fungal infections, associated with low to absent blood IgM levels, while IgG, IgG subclasses, and IgA levels, as well as IgG antibody response to vaccinations, are normal. Patients may also present allergic diatheses, and the prevalence of autoimmune diseases is increased. Disease data Klasyfikacja Disease Synonimy Selective immunoglobulin M deficiency Selektywny Niedobór immunoglobuliny M Kod ORPHA 331235 Kod OMIM - Kod ICD10 D80.4 Kod ICD11 4A01.04 *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl