Аутосомно-домінантна вторинна поліцитемія
ORPHA:247511· ICD-10 D75.1· Autosomal dominant secondary polycythemia
Визначення(English summary)
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.
- Поширеність
- Unknown
- Успадкування
- Autosomal dominant
- Вік початку
- Infancy, Neonatal