Cerebral venous thrombosis

Symptom Information:

Symptom ID: HPO:0005305
Synonyms:
Cerebral thrombosis [HPO:0005305]
Cerebral vein thrombosis [HPO:0005305]
Cerebral thrombosis [OMIM:Cerebral thrombosis]
Cerebral vein thrombosis [OMIM:Cerebral vein thrombosis]
Cerebral venous thrombosis [OMIM:Cerebral venous thrombosis]
Cerebral thrombosis (1 patient) [OMIM:Cerebral thrombosis (1 patient)]
Cerebral thrombosis (e.g. 612283.0014 protein C deficiency) [OMIM:Cerebral thrombosis (e.g. 612283.0014 protein C deficiency)]
Cerebral venous thrombosis [MedDRA:10008138]
Cerebral thrombosis [MedDRA:10008132]
Quality:
Cross references:
OMIM: "Cerebral thrombosis" [OMIM:Cerebral thrombosis]
OMIM: "Cerebral vein thrombosis" [OMIM:Cerebral vein thrombosis]
OMIM: "Cerebral venous thrombosis" [OMIM:Cerebral venous thrombosis]
OMIM: "Cerebral thrombosis (1 patient)" [OMIM:Cerebral thrombosis (1 patient)]
OMIM: "Cerebral thrombosis (e.g. 612283.0014 protein C deficiency)" [OMIM:Cerebral thrombosis (e.g. 612283.0014 protein C deficiency)]
Is a (Direct Parents):
MedDRA Cerebrovascular embolism and thrombosis
MedDRA Cerebrovascular venous and sinus thrombosis
HPO         Venous 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)
                Cerebral venous thrombosis(HPO:0005305)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Thromboembolism(HPO:0001907)
       Cerebrovascular embolism and thrombosis(MedDRA:10008205)
          Cerebral venous thrombosis(HPO:0005305)
Nervous system disorders(MedDRA:10029205)
    Central nervous system vascular disorders(MedDRA:10007963)
       Cerebrovascular venous and sinus thrombosis(MedDRA:10008209)
          Cerebral venous thrombosis(HPO:0005305)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Hereditary thrombophilia due to congenital antithrombin deficiency (Orphanet:82)
Hereditary thrombophilia due to congenital protein C deficiency (Orphanet:745)
PGM1-CDG (Orphanet:319646)
Protein S acquired deficiency (Orphanet:26349)
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL DOMINANT (OMIM:176860)
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE (OMIM:614514)
THROMBOPHILIA DUE TO THROMBIN DEFECT (OMIM:188050)