Myeloproliferative disorder

Symptom Information:

Symptom ID: HPO:0005547
Synonyms:
Myeloproliferative syndrome [Orphanet:51080]
Myeloproliferative disorder [OMIM:Myeloproliferative disorder]
Myeloproliferative syndrome/chronic leukemia [Orphanet:51080]
Myeloproliferative disorders (excl leukaemias) [MedDRA:10028578]
Myeloproliferative disorder [MedDRA:10028576]
Quality:
Cross references:
Orphanet:51080 "Myeloproliferative syndrome/chronic leukemia" [Orphanet:51080]
OMIM: "Myeloproliferative disorder" [OMIM:Myeloproliferative disorder]
Is a (Direct Parents):
MedDRA Haematopoietic neoplasms (excl leukaemias and lymphomas)
HPO         Leukemia
Orphanet Haematological malignancy
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of cellular immune system(HPO:0010987)
             Abnormality of leukocytes(HPO:0001881)
                Leukemia(HPO:0001909)
                   Myeloproliferative disorder(HPO:0005547)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Hematological neoplasm(HPO:0004377)
             Leukemia(HPO:0001909)
                Myeloproliferative disorder(HPO:0005547)
          Abnormality of leukocytes(HPO:0001881)
             Leukemia(HPO:0001909)
                Myeloproliferative disorder(HPO:0005547)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Hematological neoplasm(HPO:0004377)
                Leukemia(HPO:0001909)
                   Myeloproliferative disorder(HPO:0005547)
MedDRA:
Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104)
    Haematopoietic neoplasms (excl leukaemias and lymphomas)(MedDRA:10018865)
       Myeloproliferative disorder(HPO:0005547)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Down syndrome (Orphanet:870)
Essential thrombocythemia (Orphanet:3318)
Idiopathic hypereosinophilic syndrome (Orphanet:3260)
MYELOPROLIFERATIVE DISEASE, AUTOSOMAL RECESSIVE (OMIM:254700)
MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA (OMIM:131440)
Myelofibrosis with myeloid metaplasia (Orphanet:824)
Noonan syndrome (Orphanet:648)