Heterotaxy, visceral, 5, autosomal

Definition

Any visceral hetetotaxy in which the cause of the disease is a mutation in the NODAL gene.

Also known as HTX5, NODAL visceral heterotaxy, situs inversus viscerum, SIV, visceral heterotaxy caused by mutation in NODAL — per MONDO

Also identified as

• OMIM 270100 per MONDO
• UMLS C3495537 per MONDO