Thrombocytosis

Symptom Information:

Symptom ID: HPO:0001894
Synonyms:
Increased platelet count [HPO:0001894]
thrombocytosis [HPO:0001894]
Thrombocytosis [OMIM:Thrombocytosis]
Thrombocytosis (in some patients) [OMIM:Thrombocytosis (in some patients)]
Platelet count increased [MedDRA:10051608]
Thrombocytosis [MedDRA:10043563]
Quality:
Cross references:
OMIM: "Thrombocytosis" [OMIM:Thrombocytosis]
OMIM: "Thrombocytosis (in some patients)" [OMIM:Thrombocytosis (in some patients)]
UMLS:C0836924 "thrombocytosis" [HPO:0001894]
Is a (Direct Parents):
MedDRA Platelet analyses
MedDRA Thrombocytoses
HPO         Abnormal platelet count
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of thrombocytes(HPO:0001872)
             Abnormal platelet count(HPO:0011873)
                Thrombocytosis(HPO:0001894)
MedDRA:
Investigations(MedDRA:10022891)
    Haematology investigations (incl blood groups)(MedDRA:10018851)
       Platelet analyses(MedDRA:10035523)
          Thrombocytosis(HPO:0001894)
Blood and lymphatic system disorders(MedDRA:10005329)
    Abnormality of thrombocytes(HPO:0001872)
       Thrombocytoses(MedDRA:10069776)
          Thrombocytosis(HPO:0001894)
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant severe congenital neutropenia (Orphanet:486)
Blackfan-Diamond anemia (Orphanet:124)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
DIAMOND-BLACKFAN ANEMIA 1 (OMIM:105650)
Essential thrombocythemia (Orphanet:3318)
Familial isolated congenital asplenia (Orphanet:101351)
Neutropenia, severe congenital, 1, autosomal dominant (OMIM:202700)
PMM2-CDG (Orphanet:79318)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Polycythemia vera (Orphanet:729)
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET (OMIM:615934)
Syndromic diarrhea (Orphanet:84064)
THROMBOCYTHEMIA 2 (OMIM:601977)
THROMBOCYTHEMIA 3 (OMIM:614521)
THROMBOCYTHEMIA, X-LINKED (OMIM:300331)
TRICHOHEPATOENTERIC SYNDROME 1 (OMIM:222470)