Abnormality of thrombocytes

Symptom Information:

Symptom ID: HPO:0001872
Synonyms:
Blood platelet disease [HPO:0001872]
Platelet abnormalities [HPO:0001872]
Thrombasthenia [HPO:0001872]
Platelets disorder [Orphanet:48580]
Platelet disorder (disorder) [Orphanet:48580]
Blood Platelet Disorders [Orphanet:48580]
Platelet abnormalities [OMIM:Platelet abnormalities]
Thrombasthenia [OMIM:Thrombasthenia]
Platelet disorders/thrombopathies [Orphanet:48580]
Platelet disorder [Orphanet:48580]
Platelet disorder [MedDRA:10035532]
Abnormal platelets [MedDRA:10035532]
Disorder platelet [MedDRA:10035532]
Platelet abnormalities [MedDRA:10035532]
Platelet abnormalities NOS [MedDRA:10035532]
Platelet changes [MedDRA:10035532]
Platelets abnormal [MedDRA:10035532]
Qualitative platelet defects [MedDRA:10035532]
Thrombocytes abnormal (NOS) [MedDRA:10035532]
Thrombocytopathy [MedDRA:10035532]
Thrombocytopathy [OMIM:Thrombocytopathy]
Platelet disorders [MedDRA:10035534]
Thrombasthenia [MedDRA:10043529]
Quality:
Cross references:
Orphanet:48580 "Platelet disorders/thrombopathies" [Orphanet:48580]
OMIM: "Platelet abnormalities" [OMIM:Platelet abnormalities]
OMIM: "Thrombasthenia" [OMIM:Thrombasthenia]
OMIM: "Thrombocytopathy" [OMIM:Thrombocytopathy]
UMLS:C0040015 "Thrombasthenia" [HPO:0001872]
UMLS:C0005818 "Blood Platelet Disorders" [Orphanet:48580]
Is a (Direct Parents):
MedDRA Blood and lymphatic system disorders
Orphanet Abnormality of blood and blood-forming tissues
MedDRA Platelet disorders NEC
HPO         Abnormality of blood and blood-forming tissues
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)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Abnormality of thrombocytes(HPO:0001872)
Database Frequency: 20 / 7739
Resource:

All diseases associated with this symptom:

22q11.2 deletion syndrome (Orphanet:567)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
BLEEDING DISORDER, PLATELET-TYPE, 17 (OMIM:187900)
CINCA syndrome (Orphanet:1451)
Castleman disease (Orphanet:160)
Dyschromatosis universalis hereditaria 1 (OMIM:127500)
Dyschromatosis universalis hereditaria 2 (OMIM:612715)
Dyschromatosis universalis hereditaris 3 (OMIM:615402)
Ehlers-Danlos syndrome, fibronectinemic type (Orphanet:75501)
Erythromelalgia (Orphanet:1956)
Essential thrombocythemia (Orphanet:3318)
Familial thrombocytosis (Orphanet:71493)
Giant cell arteritis (Orphanet:397)
Gray platelet syndrome (Orphanet:721)
Hermansky-Pudlak syndrome (Orphanet:79430)
Mediterranean macrothrombocytopenia (Orphanet:101022)
Progressive familial intrahepatic cholestasis (Orphanet:172)
Pseudoxanthoma elasticum (Orphanet:758)
Sitosterolemia (Orphanet:2882)
Stormorken-Sjaastad-Langslet syndrome (Orphanet:3204)