Hypercoagulability

Symptom Information:

Symptom ID: HPO:0100724
Synonyms:
Blood hyperviscosity [HPO:0100724]
Thrombophilia [HPO:0100724]
Blood hypercoagulability [Orphanet:48860]
Hyperviscosity (finding) [Orphanet:48860]
Hypercoagulability state (finding) [Orphanet:48860]
Hyperviscosity [Orphanet:48860]
Blood hyperviscosity/hypercoagulability [Orphanet:48860]
Quality:
Cross references:
Orphanet:48860 "Blood hyperviscosity/hypercoagulability" [Orphanet:48860]
UMLS:C0221104 "Hyperviscosity" [Orphanet:48860]
Is a (Direct Parents):
Orphanet Abnormal bleeding
HPO         Abnormality of coagulation
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)