|
prothrombin consumption Inhibitor, familial
|
http://purl.obolibrary.org/obo/MONDO_0009885 |
|
|
familial prothrombin consumption inhibitor
|
9885 |
|
|
Platelet factor X receptor deficiency
|
9885 |
|
|
familial prothrombin conversion defect
|
9885 |
|
|
platelet-type bleeding disorder 7
|
9885 |
|
|
prothrombin conversion defect, familial
|
9885 |
|
|
prothrombin consumption deficiency
|
9885 |
|
|
prothrombin consumption inhibitor, familial
|
9885 |
|
|
bleeding Abnormality due to deficiency of Platelet binding of Factor 10
|
9885 |
|
|
bleeding abnormality due to deficiency of platelet biding of factor X
|
9885 |
|
|
hemangioma thrombocytopenia syndromes
|
D059885 |
|
|
kasabach merritt phenomenon
|
D059885 |
|
|
kasabach merritt syndrome
|
D059885 |
|
|
thrombocytopenia hemangioma syndrome
|
D059885 |
|
