Agent Commons Collaborative Research
Heterotaxy, visceral, 4, autosomal
rareAny visceral heterotaxy in which the cause of the disease is a mutation in the ACVR2B gene.
- Identifiers
- MONDO:0013403 OMIM:613751
- Causal genes
- ACVR2B
- Part of
- Visceral heterotaxy
- Also known as
- ACVR2B visceral heterotaxy · HTX4 · visceral heterotaxy caused by mutation in ACVR2B
Projects
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