Reduced kininogen activity

Symptom Information:

Symptom ID: HPO:0005527
Synonyms:
Fitzgerald factor deficiency [HPO:0005527]
Kininogen deficiency [HPO:0005527]
Williams factor deficiency [HPO:0005527]
Williams-Fitzgerald-Flaujeac factor deficiency [HPO:0005527]
Fitzgerald factor deficiency [OMIM:Fitzgerald factor deficiency]
Kininogen deficiency [OMIM:Kininogen deficiency]
Williams factor deficiency [OMIM:Williams factor deficiency]
Quality:
Cross references:
OMIM: "Fitzgerald factor deficiency" [OMIM:Fitzgerald factor deficiency]
OMIM: "Kininogen deficiency" [OMIM:Kininogen deficiency]
OMIM: "Williams factor deficiency" [OMIM:Williams factor deficiency]
Is a (Direct Parents):
HPO         Abnormality of the intrinsic pathway
HPO         Abnormality of the kinin-kallikrein system
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 kininogen activity(HPO:0005527)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of circulating protein level(HPO:0010876)
             Abnormality of the kinin-kallikrein system(HPO:0005559)
                Reduced kininogen activity(HPO:0005527)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Congenital high-molecular-weight kininogen deficiency (Orphanet:483)