Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Parent Terms Term With Siblings Child Terms
essential thrombocythemia  
familial erythrocytosis 1  
familial erythrocytosis 2  
familial erythrocytosis 3  
familial erythrocytosis 4  
familial erythrocytosis 5  
Familial Erythrocytosis 6  
Familial Erythrocytosis 7  
myeloproliferative disorder with eosinophilia  
polycythemia vera +   
A myeloproliferative disorder of unknown etiology, characterized by abnormal proliferation of all hematopoietic bone marrow elements and an absolute increase in red cell mass and total blood volume, associated frequently with splenomegaly, leukocytosis, and thrombocythemia. Hematopoiesis is also reactive in extramedullary sites (liver and spleen). In time myelofibrosis occurs.
transient myeloproliferative syndrome  

Exact Synonyms: Erythremia ;   Osler Vaquez Disease ;   Osler-Vaquez syndrome ;   PRV ;   PV ;   Polycythemia Ruba Vera ;   Polycythemia Ruba Veras ;   Polycythemia Rubra Vera ;   erythremias ;   polycythaemia rubra vera ;   polycythemia rubra veras ;   proliferative polycythaemia
Primary IDs: MESH:D011087
Alternate IDs: OMIM:263300 ;   RDO:0006388
Xrefs: GARD:7422 ;   NCI:C3336
Definition Sources: MESH:D011087,,,

paths to the root


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.