Prolonged partial thromboplastin time

Symptom Information:

Symptom ID: HPO:0003645
Synonyms:
Abnormal partial thromboplastin time [HPO:0003645]
Delayed thromboplastin generation [HPO:0003645]
Partial thromboplastin time prolonged [HPO:0003645]
Prolonged activated partial thromboplastin time [HPO:0003645]
Abnormal partial thromboplastin time [OMIM:Abnormal partial thromboplastin time]
Partial thromboplastin time prolonged [OMIM:Partial thromboplastin time prolonged]
Prolonged activated partial thromboplastin time [OMIM:Prolonged activated partial thromboplastin time]
Prolonged partial thromboplastin time [OMIM:Prolonged partial thromboplastin time]
Prolonged activated partial thromboplastin time (APTT) [OMIM:Prolonged activated partial thromboplastin time (APTT)]
Prolonged activated partial thromboplastin time (aPTT) [OMIM:Prolonged activated partial thromboplastin time (aPTT)]
Prolonged partial thromboplastin time (PTT) [OMIM:Prolonged partial thromboplastin time (PTT)]
Activated partial thromboplastin time prolonged [MedDRA:10000636]
Quality:
Cross references:
OMIM: "Abnormal partial thromboplastin time" [OMIM:Abnormal partial thromboplastin time]
OMIM: "Partial thromboplastin time prolonged" [OMIM:Partial thromboplastin time prolonged]
OMIM: "Prolonged activated partial thromboplastin time" [OMIM:Prolonged activated partial thromboplastin time]
OMIM: "Prolonged partial thromboplastin time" [OMIM:Prolonged partial thromboplastin time]
OMIM: "Prolonged activated partial thromboplastin time (APTT)" [OMIM:Prolonged activated partial thromboplastin time (APTT)]
OMIM: "Prolonged activated partial thromboplastin time (aPTT)" [OMIM:Prolonged activated partial thromboplastin time (aPTT)]
OMIM: "Prolonged partial thromboplastin time (PTT)" [OMIM:Prolonged partial thromboplastin time (PTT)]
Is a (Direct Parents):
MedDRA Coagulation and bleeding analyses
HPO         Abnormality of coagulation
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)
             Prolonged partial thromboplastin time(HPO:0003645)
MedDRA:
Investigations(MedDRA:10022891)
    Haematology investigations (incl blood groups)(MedDRA:10018851)
       Coagulation and bleeding analyses(MedDRA:10009728)
          Prolonged partial thromboplastin time(HPO:0003645)
Database Frequency: 20 / 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)
Congenital factor XI deficiency (Orphanet:329)
Congenital factor XII deficiency (Orphanet:330)
Congenital high-molecular-weight kininogen deficiency (Orphanet:483)
Congenital prekallikrein deficiency (Orphanet:749)
DPM1-CDG (Orphanet:79322)
FACTORS VIII, IX AND XI, COMBINED DEFICIENCY OF (OMIM:134520)
Familial hemophagocytic lymphohistiocytosis (Orphanet:540)
HEMOPHILIA A (OMIM:306700)
Hemophilia B (Orphanet:98879)
Hereditary combined deficiency of vitamin K-dependent clotting factors (Orphanet:98434)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
PASSOVOY FACTOR DEFECT (OMIM:168830)
PMM2-CDG (Orphanet:79318)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (Orphanet:88618)
THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE (OMIM:188055)
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1 (OMIM:277450)