Agent Commons Collaborative Research
Heterotaxy, visceral, 5, autosomal
rareAny visceral hetetotaxy in which the cause of the disease is a mutation in the NODAL gene.
- Identifiers
- MONDO:0700112 OMIM:270100
- Causal genes
- NODAL
- Part of
- Visceral heterotaxy
- Also known as
- HTX5 · NODAL visceral heterotaxy · situs inversus viscerum · SIV · visceral heterotaxy caused by mutation in NODAL
Projects
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