Reduced factor VIII activity

Symptom Information:

Symptom ID: HPO:0003125
Synonyms:
Factor VIII deficiency [HPO:0003125]
Factor VIII deficiency [OMIM:Factor VIII deficiency]
Factor VIII deficiency [MedDRA:10016080]
Quality:
Cross references:
OMIM: "Factor VIII deficiency" [OMIM:Factor VIII deficiency]
Is a (Direct Parents):
MedDRA Coagulation factor deficiencies
HPO         Abnormality of the intrinsic pathway
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)
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)