Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja An extremely rare slow-growing glial neoplasm of the central nervous system, usually arising in a superficial location in the cerebrum, affecting all ages and both sexes, and characterized by intractable seizures and headaches, with most cases being cured by surgical incision alone and therefore having a good prognosis. Disease data Klasyfikacja Disease Kod ORPHA 251671 Kod OMIM - Kod ICD10 C71.9 Kod ICD11 2A00.0Y *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