Prolonged partial thromboplastin time
Symptom Information:
Symptom ID: | HPO:0003645 | ||||||||||||
Synonyms: |
|
||||||||||||
Quality: | |||||||||||||
Cross references: |
|
||||||||||||
Is a (Direct Parents): |
|
||||||||||||
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) |