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primary familial polycythemia due to EPO receptor mutation

Disease Summary
Associated Targets (3)
Tclin

2

Tbio

1


GARD Rare
Mondo Description Primary familial polycythemia is an inherited hematological disorder resulting from mutations in the erythropoietin (EPO) receptor and is characterized by an elevated absolute red blood cell mass caused by uncontrolled red blood cell production in the presence of low EPO levels.
Uniprot Description An autosomal dominant disorder characterized by increased serum red blood cell mass, elevated hemoglobin and hematocrit, hypersensitivity of erythroid progenitors to erythropoietin, erythropoietin low serum levels, and no increase in platelets nor leukocytes. It has a relatively benign course and does not progress to leukemia.
Mondo Term and Equivalent IDs
MONDO:0007572:  primary familial polycythemia due to EPO receptor mutation
GARD:0009843: 
ICD9:289.6: 
Orphanet:90042: 
SCTID:17342003: