syndromic disease hereditary disease visceral heterotaxy https://github.com/monarch-initiative/mondo/issues/2826 https://github.com/monarch-initiative/mondo/issues/6740 https://www.malacards.org/card/visceral_heterotaxy icd11.foundation:780273165 UMLS:C3178805 heterotaxia incomplete situs inversus visceral heterotaxy GARD:0010875 SCTID:14821001 Orphanet:157769 lateralization defect situs ambiguous MedDRA:10059119 DOID:0050545 MEDGEN:465273 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. Orphanet:450 partial situs inversus NCIT:C117273 heterotaxy syndrome MedDRA:10067265 situs ambiguus heterotaxy, visceral MONDO:0018677 OMIMPS:306955 heterotaxia syndrome congenital heart malformation