PedAM
Pediatric Disease Annotations & Medicines
| Disease | hyperhomocysteinemia |
| Phenotype | C0856761|budd-chiari syndrome |
| 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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