Polycythemia

Symptom Information:

Symptom ID: HPO:0001901
Synonyms:
Erythrocytosis [HPO:0001901]
Erythrocytosis [Orphanet:48300]
Polycythemia [Orphanet:48300]
Erythrocytosis [OMIM:Erythrocytosis]
Polycythemia [OMIM:Polycythemia]
Polyglobulia [Orphanet:48300]
Polycythaemia [Orphanet:48300]
Polycythaemia [MedDRA:10036051]
Erythrocytosis [MedDRA:10036051]
Physiological polycythaemia [MedDRA:10036051]
Polycythaemia due to excess erythopoetin production [MedDRA:10036051]
Polycythaemia due to hypoxia [MedDRA:10036051]
Polycythaemia NOS [MedDRA:10036051]
Polycythemia [MedDRA:10036051]
Polycythemia, secondary [MedDRA:10036051]
Secondary polycythaemia [MedDRA:10036051]
Spurious polycythaemia [MedDRA:10036051]
Physiological polycythemia [MedDRA:10036051]
Polycythemia due to excess erythopoetin production [MedDRA:10036051]
Polycythemia due to hypoxia [MedDRA:10036051]
Secondary polycythemia [MedDRA:10036051]
Spurious polycythemia [MedDRA:10036051]
Polycythaemia, secondary [MedDRA:10036051]
Post transplant erythrocytosis [MedDRA:10036051]
Polyglobulia [MedDRA:10036051]
Erythrocytosis (e.g. Hb Brigham 141900.0028) [OMIM:Erythrocytosis (e.g. Hb Brigham 141900.0028)]
Polycythemia (e.g. Hb Chesapeake 141800.0018) [OMIM:Polycythemia (e.g. Hb Chesapeake 141800.0018)]
Polycythaemia (excl rubra vera) [MedDRA:10036052]
Quality:
Cross references:
Orphanet:48300 "Polyglobulia" [Orphanet:48300]
OMIM: "Erythrocytosis" [OMIM:Erythrocytosis]
OMIM: "Polycythemia" [OMIM:Polycythemia]
OMIM: "Erythrocytosis (e.g. Hb Brigham 141900.0028)" [OMIM:Erythrocytosis (e.g. Hb Brigham 141900.0028)]
OMIM: "Polycythemia (e.g. Hb Chesapeake 141800.0018)" [OMIM:Polycythemia (e.g. Hb Chesapeake 141800.0018)]
UMLS:C1527405 "Erythrocytosis" [HPO:0001901]
UMLS:C0032461 "Polycythemia" [Orphanet:48300]
UMLS:C1527405 "Erythrocytosis" [Orphanet:48300]
Is a (Direct Parents):
MedDRA Red blood cell disorders
HPO         Abnormality of erythrocytes
Orphanet Abnormality of erythrocytes
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of erythrocytes(HPO:0001877)
             Polycythemia(HPO:0001901)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Red blood cell disorders(MedDRA:10038158)
       Polycythemia(HPO:0001901)
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

ADENOSINE TRIPHOSPHATE, ELEVATED, OF ERYTHROCYTES (OMIM:102900)
Chuvash erythrocytosis (Orphanet:238557)
Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome (Orphanet:309854)
ERYTHROCYTOSIS, FAMILIAL, 3 (OMIM:609820)
Fumaric aciduria (Orphanet:24)
HEMOGLOBIN--ALPHA LOCUS 1 (OMIM:141800)
HEMOGLOBIN--BETA LOCUS (OMIM:141900)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Idiopathic pulmonary alveolar proteinosis (Orphanet:747)
PERICARDIAL EFFUSION, CHRONIC (OMIM:260900)
Primary familial polycythemia (Orphanet:90042)
Recessive hereditary methemoglobinemia type 1 (Orphanet:139373)
Recessive hereditary methemoglobinemia type 2 (Orphanet:139380)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER (OMIM:187300)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 (OMIM:600376)
Von Hippel-Lindau disease (Orphanet:892)