Reduced prothrombin activity
Symptom Information:
Symptom ID: | HPO:0012201 | ||
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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) Reduced prothrombin activity(HPO:0012201) MedDRA: |
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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 II deficiency | (Orphanet:325) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2 | (OMIM:607473) |