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Syndrome

Heterotaxy Syndrome

AMW:DIS:140029

Abnormal thoracoabdominal VISCERA arrangement (visceral heterotaxy) or malformation that involves additional CONGENITAL HEART DEFECTS (e.g., heart isomerism; DEXTROCARDIA) and/or abnormal SPLEEN (e.g., asplenia and polysplenia). Irregularities with the central nervous system, the skeleton and urinary tract are often associated with the syndrome.

Pathology clinical
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Heterotaxy Syndrome has parent Abnormalities, Multiple
Heterotaxy Syndrome has parent Heart Defects, Congenital
Heterotaxy Syndrome has parent Splenic Diseases

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