Reduced factor VIII activity
Symptom Information:
Symptom ID: | HPO:0003125 | ||||
Synonyms: |
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Cross references: |
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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) Abnormality of coagulation(HPO:0001928) Abnormality of the coagulation cascade(HPO:0003256) Abnormality of the intrinsic pathway(HPO:0010989) Reduced factor VIII activity(HPO:0003125) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Coagulopathies and bleeding diatheses (excl thrombocytopenic)(MedDRA:10064477) Coagulation factor deficiencies(MedDRA:10009737) Reduced factor VIII activity(HPO:0003125) |
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Database Frequency: | 13 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Combined deficiency of factor V and factor VIII | (Orphanet:35909) |
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 | (OMIM:227300) |
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 | (OMIM:613625) |
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, WITH NORMAL PROTEINC AND PROTEIN C INHIBITOR | (OMIM:227310) |
FACTOR VII AND FACTOR VIII, COMBINED DEFICIENCY OF | (OMIM:134430) |
FACTOR VIII AND FACTOR IX, COMBINED DEFICIENCY OF | (OMIM:134510) |
FACTOR VIII DEFICIENCY | (OMIM:134500) |
HEMOPHILIA A | (OMIM:306700) |
HEMOPHILIA A WITH VASCULAR ABNORMALITY | (OMIM:306800) |
Hemophilia A | (Orphanet:98878) |
Noonan syndrome | (Orphanet:648) |
Von Willebrand disease type 1 | (Orphanet:166078) |
Von Willebrand disease type 3 | (Orphanet:166096) |