Reduced factor XI activity

Symptom Information:

Symptom ID: HPO:0001929
Synonyms:
Factor XI deficiency [HPO:0001929]
Factor XI deficiency [OMIM:Factor XI deficiency]
Factor XI deficiency [MedDRA:10016082]
Quality:
Cross references:
OMIM: "Factor XI deficiency" [OMIM:Factor XI 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 XI activity(HPO:0001929)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Coagulopathies and bleeding diatheses (excl thrombocytopenic)(MedDRA:10064477)
       Coagulation factor deficiencies(MedDRA:10009737)
          Reduced factor XI activity(HPO:0001929)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

ALG6-CDG (Orphanet:79320)
Congenital factor XI deficiency (Orphanet:329)
FACTOR IX AND FACTOR XI, COMBINED DEFICIENCY OF (OMIM:134540)
MGAT2-CDG (Orphanet:79329)
MPI-CDG (Orphanet:79319)
Noonan syndrome (Orphanet:648)
PMM2-CDG (Orphanet:79318)