Prolonged prothrombin time

Symptom Information:

Symptom ID: HPO:0008151
Synonyms:
Prolonged prothrombin time [OMIM:Prolonged prothrombin time]
Prolonged prothrombin time (PT) [OMIM:Prolonged prothrombin time (PT)]
Prothrombin time prolonged [MedDRA:10037063]
Quality:
Cross references:
OMIM: "Prolonged prothrombin time" [OMIM:Prolonged prothrombin time]
OMIM: "Prolonged prothrombin time (PT)" [OMIM:Prolonged prothrombin time (PT)]
Is a (Direct Parents):
HPO         Abnormality of prothrombin
MedDRA Coagulation and bleeding analyses
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 prothrombin(HPO:0012200)
                   Prolonged prothrombin time(HPO:0008151)
MedDRA:
Investigations(MedDRA:10022891)
    Haematology investigations (incl blood groups)(MedDRA:10018851)
       Coagulation and bleeding analyses(MedDRA:10009728)
          Prolonged prothrombin time(HPO:0008151)
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
Congenital factor II deficiency (Orphanet:325)
Congenital factor V deficiency (Orphanet:326)
Congenital factor X deficiency (Orphanet:328)
Familial hemophagocytic lymphohistiocytosis (Orphanet:540)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 (OMIM:267700)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 (OMIM:603553)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
Neonatal hemochromatosis (Orphanet:446)
Neonatal intrahepatic cholestasis due to citrin deficiency (Orphanet:247598)
PMM2-CDG (Orphanet:79318)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (Orphanet:88618)
Reticular dysgenesis (Orphanet:33355)