Reduced factor X activity

Symptom Information:

Symptom ID: HPO:0008321
Synonyms:
Factor X deficiency [HPO:0008321]
Factor X deficiency [OMIM:Factor X deficiency]
Factor X deficiency [MedDRA:10052474]
Quality:
Cross references:
OMIM: "Factor X deficiency" [OMIM:Factor X deficiency]
Is a (Direct Parents):
HPO         Abnormality of the common coagulation 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 common coagulation pathway(HPO:0010990)
                   Reduced factor X activity(HPO:0008321)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Coagulopathies and bleeding diatheses (excl thrombocytopenic)(MedDRA:10064477)
       Coagulation factor deficiencies(MedDRA:10009737)
          Reduced factor X activity(HPO:0008321)
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency (Orphanet:91135)
Congenital factor X deficiency (Orphanet:328)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2 (OMIM:607473)