Abnormality of thrombocytes
Symptom Information:
Symptom ID: | HPO:0001872 | |||||||||||||||||||||||
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) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Abnormality of thrombocytes(HPO:0001872) |
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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) |