Deep venous thrombosis
Symptom Information:
Symptom ID: | HPO:0002625 | ||||||||||||||||||||||
Synonyms: |
|
||||||||||||||||||||||
Quality: | |||||||||||||||||||||||
Cross references: |
|
||||||||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||||||||
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) Deep venous thrombosis(HPO:0002625) MedDRA: Vascular disorders(MedDRA:10047065) Vascular inflammations(MedDRA:10047116) Phlebitis NEC(MedDRA:10052780) Deep venous thrombosis(HPO:0002625) Thromboembolism(HPO:0001907) Non-site specific embolism and thrombosis(MedDRA:10014524) Deep venous thrombosis(HPO:0002625) Peripheral embolism and thrombosis(MedDRA:10034572) Deep venous thrombosis(HPO:0002625) |
||||||||||||||||||||||
Database Frequency: | 10 / 7739 | ||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Cushing disease | (Orphanet:96253) |
Familial thrombomodulin anomalies | (Orphanet:3324) |
Hereditary thrombophilia due to congenital antithrombin deficiency | (Orphanet:82) |
Hereditary thrombophilia due to congenital protein C deficiency | (Orphanet:745) |
Proteus syndrome | (Orphanet:744) |
THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE | (OMIM:188055) |
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL DOMINANT | (OMIM:176860) |
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE | (OMIM:612304) |
THROMBOPHILIA DUE TO THROMBIN DEFECT | (OMIM:188050) |
THROMBOPHILIA, X-LINKED, DUE TO FACTOR IX DEFECT | (OMIM:300807) |