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Results 1 - 4 of 4 for "Heterotaxy," "visceral," "12," autosomal
  1. Heterotaxy syndrome 
    ... defect, partial, with heterotaxy syndrome Genetic Testing Registry: Heterotaxy, visceral, 5, autosomal Genetic Testing Registry: Visceral heterotaxy Genetic Testing Registry: ...
    https://medlineplus.gov/genetics/condition/heterotaxy-syndrome - Genetics
  2. Critical congenital heart disease 
    ... Registry: Hypoplastic left heart syndrome Genetic Testing Registry: Heterotaxy, visceral, 2, autosomal Genetic Testing Registry: Hypoplastic left heart syndrome 2 ...
    https://medlineplus.gov/.../critical-congenital-heart-disease - Genetics
  3. Primary ciliary dyskinesia 
    ... are often said to have Kartagener syndrome.Approximately 12 percent of people with primary ciliary dyskinesia have a condition known as heterotaxy syndrome or situs ambiguus, which is characterized by abnormalities ...
    https://medlineplus.gov/.../condition/primary-ciliary-dyskinesia - Genetics
  4. GJA1 gene 
    ... K, Passos-Bueno MR, Reichenberger EJ. A novel autosomal recessive GJA1 missense mutation linked to Craniometaphyseal dysplasia. PLoS One. 2013 Aug 12;8(8):e73576. doi: 10.1371/journal.pone. ...
    https://medlineplus.gov/genetics/gene/gja1 - Genetics