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Results 1 - 8 of 8 for Atrial septal defect 6
  1. MYH6 gene 
    ... is the predominant sarcomeric disease gene for familial atrial septal defects. PLoS One. 2011;6(12):e28872. doi: 10.1371/journal.pone.0028872. ...
    https://medlineplus.gov/genetics/gene/myh6 - Genetics
  2. Heterotaxy syndrome 
    ... Organization for Rare Disorders (NORD) ClinicalTrials.gov ... PubMed ...
    https://medlineplus.gov/genetics/condition/heterotaxy-syndrome - Genetics
  3. Schinzel-Giedion syndrome 
    Schinzel-Giedion syndrome is a severe condition that is apparent at birth and affects many body systems. Signs and symptoms of this condition include distinctive ...
    https://medlineplus.gov/genetics/condition/schinzel-giedion-syndrome - Genetics
  4. Holt-Oram syndrome 
    ... chambers of the heart (atria) is called an atrial septal defect (ASD), and a hole in the septum between ... Cerbai E, Sartiani L. Holt-oram syndrome and atrial fibrillation: opening the (T)-box. Circ Res. 2008 Jun 6;102(11):1304-6. doi: 10.1161/CIRCRESAHA. ...
    https://medlineplus.gov/genetics/condition/holt-oram-syndrome - Genetics
  5. Cardiofaciocutaneous syndrome 
    ... between the two upper chambers of the heart (atrial septal defect), and a form of heart disease that enlarges ...
    https://medlineplus.gov/.../condition/cardiofaciocutaneous-syndrome - Genetics
  6. Geleophysic dysplasia 
    ... between the two upper chambers of the heart (atrial septal defect).Other features of geleophysic dysplasia can include an ...
    https://medlineplus.gov/genetics/condition/geleophysic-dysplasia - Genetics
  7. Snijders Blok-Campeau syndrome 
    ... between the two upper chambers of the heart (atrial septal defect) or another problem with the heart's structure ...
    https://medlineplus.gov/.../condition/snijders-blok-campeau-syndrome - Genetics
  8. Oculofaciocardiodental syndrome 
    ... hole between two chambers of the heart (an atrial or ventricular septal defect) or a leak in one of the valves ...
    https://medlineplus.gov/.../oculofaciocardiodental-syndrome - Genetics