Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines




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).

Page: 1