Hypercoagulability
Symptom Information:
Symptom ID: | HPO:0100724 | |||||||
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) Abnormality of coagulation(HPO:0001928) Hypercoagulability(HPO:0100724) MedDRA: |
|||||||
Database Frequency: | 15 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
Babesiosis | (Orphanet:108) |
Deafness - lymphedema - leukemia | (Orphanet:3226) |
Familial thrombomodulin anomalies | (Orphanet:3324) |
Gaucher disease type 3 | (Orphanet:77261) |
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency | (Orphanet:217467) |
Hereditary thrombophilia due to congenital protein C deficiency | (Orphanet:745) |
Klippel-Trénaunay syndrome | (Orphanet:90308) |
Protein S acquired deficiency | (Orphanet:26349) |
Sneddon syndrome | (Orphanet:820) |
THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE | (OMIM:188055) |
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE | (OMIM:612304) |
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE | (OMIM:614514) |
THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGENACTIVATOR | (OMIM:612348) |
THROMBOPHILIA, X-LINKED, DUE TO FACTOR IX DEFECT | (OMIM:300807) |
Waldenström macroglobulinemia | (Orphanet:33226) |