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Results 1 - 4 of 4 for "Heterotaxy," "visceral," "4," autosomal
  1. Heterotaxy syndrome 
    ... Registry: Heterotaxy, visceral, 2, autosomal Genetic Testing Registry: Heterotaxy, visceral, 4, autosomal Genetic Testing Registry: Heterotaxy, visceral, 6, autosomal Heterotaxia ...
    https://medlineplus.gov/genetics/condition/heterotaxy-syndrome - Genetics
  2. Critical congenital heart disease 
    ... TRANSPOSITION OF THE GREAT ARTERIES, DEXTRO-LOOPED; DTGA HETEROTAXY, VISCERAL, 2, AUTOSOMAL; HTX2 ... heart disease: the glass half empty. Circ Res. 2013 Feb 15;112(4):707-20. doi: 10.1161/CIRCRESAHA.112.300853. ...
    https://medlineplus.gov/.../critical-congenital-heart-disease - Genetics
  3. GJA1 gene 
    ... Eur J Med Genet. 2005 Oct-Dec;48(4):377-87. doi: 10.1016/j.ejmg.2005.05.003. Citation on PubMed Hu Y, Chen IP, de Almeida S, Tiziani V, Do Amaral CM, Gowrishankar K, Passos-Bueno MR, Reichenberger EJ. A novel autosomal recessive GJA1 missense mutation linked to Craniometaphyseal dysplasia. ...
    https://medlineplus.gov/genetics/gene/gja1 - Genetics
  4. Primary ciliary dyskinesia 
    ... primary ciliary dyskinesia have a condition known as heterotaxy syndrome or situs ambiguus, which is characterized by abnormalities ... a spleen (asplenia) or have multiple spleens (polysplenia). Heterotaxy syndrome results from problems establishing the left and right ...
    https://medlineplus.gov/.../condition/primary-ciliary-dyskinesia - Genetics