Reduced factor XII activity

Symptom Information:

Symptom ID: HPO:0004841
Synonyms:
Factor XII deficiency [HPO:0004841]
Hageman factor deficiency [HPO:0004841]
Factor XII deficiency [OMIM:Factor XII deficiency]
Hageman factor deficiency [OMIM:Hageman factor deficiency]
Factor XII deficiency [MedDRA:10051806]
Quality:
Cross references:
OMIM: "Factor XII deficiency" [OMIM:Factor XII deficiency]
OMIM: "Hageman factor deficiency" [OMIM:Hageman factor deficiency]
Is a (Direct Parents):
HPO         Abnormality of the intrinsic pathway
MedDRA Coagulation factor deficiencies
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 XII activity(HPO:0004841)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Coagulopathies and bleeding diatheses (excl thrombocytopenic)(MedDRA:10064477)
       Coagulation factor deficiencies(MedDRA:10009737)
          Reduced factor XII activity(HPO:0004841)
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Congenital factor XII deficiency (Orphanet:330)
MGAT2-CDG (Orphanet:79329)
Noonan syndrome (Orphanet:648)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)