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Results 1 - 8 of 8 for Atrial septal defect 1
  1. Heterotaxy syndrome 
    ... Organization for Rare Disorders (NORD) ClinicalTrials.gov RIGHT ATRIAL ISOMERISM; RAI HETEROTAXY, VISCERAL, 5, AUTOSOMAL; HTX5 HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1 ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2; AVSD2 HETEROTAXY, VISCERAL, 2, AUTOSOMAL; ...
    https://medlineplus.gov/genetics/condition/heterotaxy-syndrome - Genetics
  2. MYH6 gene 
    ... heavy polypeptide 6, cardiac muscle, alpha (cardiomyopathy, hypertrophic 1) myosin-6 SSS3 ... NCBI Gene ClinVar Carniel E, Taylor ...
    https://medlineplus.gov/genetics/gene/myh6 - 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 ... Erratum In: Cardiovasc Res. 2011 Jan 1;89(1):253. Mathijssen, Inge B [added]. Citation on PubMed Cerbai E, Sartiani L. Holt-oram syndrome and atrial fibrillation: opening the (T)-box. Circ Res. 2008 ...
    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 ... with OFCD syndrome. MCOPS2 Microphthalmia, cataracts, radiculomegaly, and ... Gorlin RJ, Marashi AH, Obwegeser HL. Oculo-facio-cardio-dental (OFCD) syndrome. Am J Med Genet. 1996 May 3;63(1):290-2. doi: 10.1002/(SICI)1096-8628( ...
    https://medlineplus.gov/.../oculofaciocardiodental-syndrome - Genetics