Disease | budd-chiari syndrome |
Phenotype | C0598608|hyperhomocysteinemia |
Sentences | 1 |
PubMedID- 24773704 | Aim: a systematic review and meta-analysis were conducted to explore the role of the methylenetetrahydrofolate reductase (mthfr) c677t gene mutation and hyperhomocysteinemia in patients with budd-chiari syndrome (bcs) and portal vein thrombosis (pvt). |
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