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Results 1 - 8 of 8 for Atrial septal defect 3
  1. MYH6 gene 
    ... FAMILIAL HYPERTROPHIC, 14; CMH14 CARDIOMYOPATHY, DILATED, 1EE; CMD1EE ATRIAL SEPTAL DEFECT 3; ASD3 NCBI Gene ClinVar Carniel E, Taylor MR, ...
    https://medlineplus.gov/genetics/gene/myh6 - Genetics
  2. Heterotaxy syndrome 
    ... Organization for Rare Disorders (NORD) ... HETEROTAXY, VISCERAL, 3, AUTOSOMAL; HTX3 HETEROTAXY, VISCERAL, 6, AUTOSOMAL; HTX6 HETEROTAXY, ...
    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. McKusick-Kaufman syndrome 
    ... individuals with McKusick-Kaufman syndrome can include an atrial septal defect or a ventricular septal defect, which are openings ...
    https://medlineplus.gov/genetics/condition/mckusick-kaufman-syndrome - Genetics
  5. Holt-Oram syndrome 
    ... chambers of the heart (atria) is called an atrial septal defect (ASD), and a hole in the septum between ...
    https://medlineplus.gov/genetics/condition/holt-oram-syndrome - Genetics
  6. 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
  7. 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
  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