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QuickView for ventricular septal defect (phenotype)


Genetic Markers

Most Correlated Genes

Most Correlated SNPs

  1. ZFPM2
  2. GDF1
  3. NKX2-5
  4. JAG1
  1. No SNPs found
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Pathway Enrichment

Most Correlated Biogroups

  1. heart morphogenesis
  2. blood vessel morphogenesis
  3. vasculature development
  4. heart development
  5. cardiovascular system development
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Curated Studies

Most Correlated Studies

  1. Ventricle biopsies of cyanotic Tetralogy of Fallot patients after normoxic heart surgery
  2. Mouse Phenotypes - Congenital disorder
  3. Cyanosis-specific ventricular gene expression profiles in fallot tetralogy
  4. OMIM - Congenital disorder
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Literature

Most Relevant Literature

  1. Characterization of blood-mimicking fluids for echocardiography imaging of ventricular septal defect…
  2. Increased incidence of postmyocardial infarction ventricular septal defects during Covid-19 pandemic…
  3. Application of Mivacurium in Fast-Track Anesthesia for Transthoracic Device Closure of Ventricular S…
  4. Association Between Deleterious SCN5A Variants and Ventricular Septal Defect in Young Patients With …
  5. Maternal serum-derived exosomal lactoferrin as a marker in detecting and predicting ventricular sept…
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Clinical Trials

Most Relevant Clinical Trials

  1. Closure of Muscular Ventricular Septal Defects With The AMPLATZER™ Muscular VSD Occluder
  2. Transcatheter Versus Surgical Closure of Ventricular Septal Defect: A Comparative Study
  3. Closure of Perimembranous Ventricular Septal Defects With The AMPLATZER® Membranous VSD OCCLUDER
  4. Transcatheter Closure Versus Surgery of Perimembranous Ventricular Septal Defects
  5. A Randomized Controlled Trial:Treatments on Infundibular Ventricular Septal Defect
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