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PedAM

Pediatric Disease Annotations & Medicines




Disease thrombophilia
Phenotype C0027051|myocardial infarction (mi)
Sentences 1
PubMedID- 20642359 Background: myocardial infarction (mi) can be due to inherited thrombophilia caused by resistance to activated protein c resulting from factor v leiden (fvl) mutation.

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