Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare, genetic, hematologic disease characterized by increased levels of serum hemoglobin, hematocrit and erythrocyte mass, associated with elevated or inappropriately normal erythropoietin serum levels, occurring in various members of a family and with autosomal dominant inheritance. Disease data Classification Disease Synonyms Autosomal dominant secondary erythrocytosis Autosomalna dominująca wtórna erytrocytoza ORPHA code 247511 OMIM code 611783 ICD10 code D75.1 ICD11 code - *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