Venous thrombosis

Symptom Information:

Symptom ID: HPO:0004936
Synonyms:
Vein thrombosis [Orphanet:35450]
Phlebitis (disorder) [Orphanet:35450]
Venous thrombosis (disorder) [Orphanet:35450]
Phlebitis and thrombophlebitis (disorder) [Orphanet:35450]
Thrombophlebitis (disorder) [Orphanet:35450]
Thrombophlebitis [Orphanet:35450]
Phlebitis [Orphanet:35450]
Phlebitis and thrombophlebitis [Orphanet:35450]
Venous Thrombosis [Orphanet:35450]
Venous thrombosis [OMIM:Venous thrombosis]
Venous thrombosis/phlebitis/thrombophlebitis [Orphanet:35450]
Venous thrombosis [Orphanet:35450]
Venous thrombosis [MedDRA:10047249]
Phlebothrombosis [MedDRA:10047249]
Thrombosis venous [MedDRA:10047249]
Venous thrombosis NOS [MedDRA:10047249]
Phlebitis [MedDRA:10034879]
Thrombophlebitis [MedDRA:10043570]
Quality:
Cross references:
HPO:0002625 "Deep venous thrombosis" [Orphanet:35450]
HPO:0004418 "Thrombophlebitis" [Orphanet:35450]
Orphanet:35450 "Venous thrombosis/phlebitis/thrombophlebitis" [Orphanet:35450]
OMIM: "Venous thrombosis" [OMIM:Venous thrombosis]
UMLS:C0040046 "Thrombophlebitis" [Orphanet:35450]
UMLS:C0031542 "Phlebitis" [Orphanet:35450]
UMLS:C1367972 "Phlebitis and thrombophlebitis" [Orphanet:35450]
UMLS:C0042487 "Venous Thrombosis" [Orphanet:35450]
Is a (Direct Parents):
MedDRA Phlebitis NEC
HPO         Abnormal thrombosis
MedDRA Peripheral embolism and thrombosis
HPO         Splanchnic vein thrombosis
Orphanet Abnormality of cardiovascular system physiology
MedDRA Non-site specific embolism and 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)
             Venous thrombosis(HPO:0004936)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular inflammations(MedDRA:10047116)
       Phlebitis NEC(MedDRA:10052780)
          Venous thrombosis(HPO:0004936)
    Thromboembolism(HPO:0001907)
       Peripheral embolism and thrombosis(MedDRA:10034572)
          Venous thrombosis(HPO:0004936)
       Non-site specific embolism and thrombosis(MedDRA:10014524)
          Venous thrombosis(HPO:0004936)
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)