Venous thrombosis
Symptom Information:
Symptom ID: | HPO:0004936 | ||||||||||||||||||
Synonyms: |
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Cross references: |
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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) Venous thrombosis(HPO:0004936) MedDRA: Vascular disorders(MedDRA:10047065) Vascular inflammations(MedDRA:10047116) Phlebitis NEC(MedDRA:10052780) Venous thrombosis(HPO:0004936) Thromboembolism(HPO:0001907) Non-site specific embolism and thrombosis(MedDRA:10014524) Venous thrombosis(HPO:0004936) Peripheral embolism and thrombosis(MedDRA:10034572) Venous thrombosis(HPO:0004936) |
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Database Frequency: | 41 / 7739 | ||||||||||||||||||
Resource: |
All diseases associated with this symptom:
48,XXXY syndrome | (Orphanet:96263) |
49,XXXXY syndrome | (Orphanet:96264) |
ANTIPHOSPHOLIPID SYNDROME, FAMILIAL | (OMIM:107320) |
Angio-osteohypertrophic syndrome | (Orphanet:2346) |
Babesiosis | (Orphanet:108) |
Behçet disease | (Orphanet:117) |
Beta-thalassemia | (Orphanet:848) |
Beta-thalassemia intermedia | (Orphanet:231222) |
Beta-thalassemia major | (Orphanet:231214) |
Classical homocystinuria | (Orphanet:394) |
Cushing disease | (Orphanet:96253) |
Enchondromatosis | (Orphanet:296) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Essential thrombocythemia | (Orphanet:3318) |
Familial dysfibrinogenemia | (Orphanet:98881) |
Familial multiple nevi flammei | (Orphanet:624) |
Familial thrombocytosis | (Orphanet:71493) |
Granulomatosis with polyangiitis | (Orphanet:900) |
Hereditary hemorrhagic telangiectasia | (Orphanet:774) |
Hereditary thrombophilia due to congenital protein C deficiency | (Orphanet:745) |
Hereditary thrombophilia due to congenital protein S deficiency | (Orphanet:743) |
Hughes-Stovin syndrome | (Orphanet:228116) |
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency | (Orphanet:83639) |
Idiopathic hypereosinophilic syndrome | (Orphanet:3260) |
Klatskin tumor | (Orphanet:99978) |
Klippel-Trénaunay syndrome | (Orphanet:90308) |
Maffucci syndrome | (Orphanet:163634) |
Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
Microscopic polyangiitis | (Orphanet:727) |
Neurocutaneous melanocytosis | (Orphanet:2481) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Polycythemia vera | (Orphanet:729) |
Polymyositis | (Orphanet:732) |
Primary familial polycythemia | (Orphanet:90042) |
Relapsing polychondritis | (Orphanet:728) |
SAPHO syndrome | (Orphanet:793) |
Secondary polycythemia | (Orphanet:98428) |
Systemic capillary leak syndrome | (Orphanet:188) |
THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE | (OMIM:188055) |
Thoracic outlet syndrome | (Orphanet:97330) |
Typhoid | (Orphanet:99745) |