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Visceral heterotaxy

A rare, genetic disorder in which symptoms are generally secondary to the abnormal location of the organs within the thoracic, abdominal, or peritoneal cavities. Anatomic and functional problems can include cardiac defects, intestinal malrotation leading to volvulus, biliary atresia, and various defects of the central nervous system, urinary tract, and skeleton.

1 trial tagged with this condition →

Dextrocardia 1 trial
Situs inversus 1 trial Sub-types →
Heterotaxy, visceral, 1, X-linked 0 trials
Heterotaxy, visceral, 10, autosomal, with male infertility 0 trials
Heterotaxy, visceral, 11, autosomal, with male infertility 0 trials
Heterotaxy, visceral, 12, autosomal 0 trials
Heterotaxy, visceral, 13, autosomal 0 trials
Heterotaxy, visceral, 14, autosomal 0 trials
Heterotaxy, visceral, 2, autosomal 0 trials
Heterotaxy, visceral, 3, autosomal 0 trials
Heterotaxy, visceral, 4, autosomal 0 trials
Heterotaxy, visceral, 5, autosomal 0 trials
Heterotaxy, visceral, 6, autosomal 0 trials
Heterotaxy, visceral, 7, autosomal 0 trials
Heterotaxy, visceral, 8, autosomal 0 trials
Heterotaxy, visceral, 9, autosomal, with male infertility 0 trials
Laterality defects, autosomal dominant 0 trials
Levocardia 0 trials
Right atrial isomerism 0 trials