Search for a rare disease
Other search option(s)
Autosomal dominant secondary polycythemia
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.
ORPHA:247511Classification level: Disorder