Cerebral venous thrombosis
Symptom Information:
Symptom ID: | HPO:0005305 | |||||||||
Synonyms: |
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Is a (Direct Parents): |
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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) 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) |
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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) |