Any visceral hetetotaxy in which the cause of the disease is a mutation in the NODAL gene. The disease is heterotaxy, visceral, 5, autosomal (MONDO_0700112, a Monarch Disease Ontology id). Also known as: HTX5, NODAL visceral heterotaxy, SIV, situs inversus viscerum, visceral heterotaxy caused by mutation in NODAL.