Thrombocytosis
Symptom Information:
Symptom ID: | HPO:0001894 | ||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |