Thromboembolism
Symptom Information:
Symptom ID: | HPO:0001907 | |||||||
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) Abnormal thrombosis(HPO:0001977) Thromboembolism(HPO:0001907) MedDRA: Vascular disorders(MedDRA:10047065) Thromboembolism(HPO:0001907) |
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Database Frequency: | 15 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
Adult heart tumor | (Orphanet:874) |
Atrial fibrillation, familial, 3 | (OMIM:607554) |
Atrial standstill 2 | (OMIM:615745) |
Classical homocystinuria | (Orphanet:394) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
Familial atrial myxoma | (Orphanet:615) |
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | (Orphanet:300751) |
Familial isolated dilated cardiomyopathy | (Orphanet:154) |
Familial isolated hypertrophic cardiomyopathy | (Orphanet:155) |
Loeffler endocarditis | (Orphanet:75566) |
Methylmalonic acidemia with homocystinuria, type cblC | (Orphanet:79282) |
Papillary fibroelastoma of the heart | (Orphanet:208600) |
Peripartum cardiomyopathy | (Orphanet:563) |
Polycythemia vera | (Orphanet:729) |
THROMBOPHILIA DUE TO THROMBIN DEFECT | (OMIM:188050) |