Reduced factor XIII activity

Symptom Information:

Symptom ID: HPO:0008357
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Abnormality of the common coagulation 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 common coagulation pathway(HPO:0010990)
                   Reduced factor XIII activity(HPO:0008357)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Congenital factor XIII deficiency (Orphanet:331)
FACTOR XIII, B SUBUNIT, DEFICIENCY OF (OMIM:613235)
Noonan syndrome (Orphanet:648)