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References OMIM Gene GeneReviews HGMD HGNC
last update : 22-11-2016
Symbol HTX5
Location 10q22.1
Name heterotaxy, visceral, 5
Corresponding gene NODAL
Main clinical features
  • developmental disorder characterized by complex congenital heart malformations and/or situs inversus and caused by defects in the normal left-right asymmetric positioning of internal organs
  • Genetic determination not applicable
    Function/system disorder cardiovascular
    digestive tract/gastrointestinal
    Type disease