Thromboembolism

Symptom Information:

Symptom ID: HPO:0001907
Synonyms:
Embolism and thrombosis [HPO:0001907]
Thromboembolic disease [HPO:0001907]
Thromboembolic events [HPO:0001907]
Thromboembolic events [OMIM:Thromboembolic events]
Thromboembolism [OMIM:Thromboembolism]
Thromboembolism (25%) [OMIM:Thromboembolism (25%)]
Embolism and thrombosis [MedDRA:10014523]
Quality:
Cross references:
OMIM: "Thromboembolic events" [OMIM:Thromboembolic events]
OMIM: "Thromboembolism" [OMIM:Thromboembolism]
OMIM: "Thromboembolism (25%)" [OMIM:Thromboembolism (25%)]
Is a (Direct Parents):
MedDRA Vascular disorders
HPO         Abnormal thrombosis
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)
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)