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Results 1 - 4 of 4 for "Heterotaxy," "visceral," "6," autosomal
  1. Heterotaxy syndrome 
    ... Registry: Heterotaxy, visceral, 4, autosomal Genetic Testing Registry: Heterotaxy, visceral, 6, autosomal Heterotaxia National Organization for Rare Disorders (NORD) ClinicalTrials. ...
    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 CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6; CHTD6 HYPOPLASTIC LEFT HEART SYNDROME 2; HLHS2 PubMed ...
    https://medlineplus.gov/.../critical-congenital-heart-disease - Genetics
  3. 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
  4. GJA1 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Heterotaxy syndrome More About This Health Condition Mutations in one ... K, Passos-Bueno MR, Reichenberger EJ. A novel autosomal recessive GJA1 missense mutation linked to Craniometaphyseal dysplasia. ...
    https://medlineplus.gov/genetics/gene/gja1 - Genetics