Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare systemic autoimmune disease characterized by exocrine gland dysfunction, resulting predominately in keratoconjunctivitis sicca and xerostomia, but also affecting exocrine glands of the skin, as well as respiratory, urogenital, and digestive tract. Extraglandular manifestations include arthritis, interstitial lung disease, renal disease, and peripheral neuropathy. The disease is accompanied by a substantially increased risk to develop B-cell non-Hodgkin lymphoma, especially MALT (mucosa-associated lymphoid tissue) lymphoma. Disease data Klasyfikacja Disease Synonimy Primary Sjögren-Gougerot syndrome Pierwotny zespół Sjögrena-Gougerota Kod ORPHA 289390 Kod OMIM 270150 Kod ICD10 M35.0 Kod ICD11 4A43.20 *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