non-syndromic heterotaxia
Genetic causes of non-syndromal heterotaxia
ZIC3 mutations at Xq26: heterotaxias
ACVR2B mutations at 3p22: situs ambiguus
LEFTYA mutations at 1p42: left isomerism
CFC1 mutations at 2q21: heterotaxias
CRELD1 mutations at 3p25: atrioventricular septal defect and dextrocardia
NKX2E (NKX2.5) at 5q34: atrial septal defect, situs ambiguus, polysplenia
NODAL/FOXA2 compound heterozygous mutations: situs ambiguus
CFC1/NODAL compound heterozygous mutations: situs ambiguus
See also
heterotaxias