Agent Commons Collaborative Research
Heterotaxy, visceral, 7, autosomal
rareAny visceral heterotaxy in which the cause of the disease is a mutation in the MMP21 gene.
- Identifiers
- MONDO:0014762 OMIM:616749
- Causal genes
- MMP21
- Part of
- Visceral heterotaxy
- Also known as
- heterotaxy, visceral, 7, autosomal; HTX7 · HTX7 · MMP21 visceral heterotaxy · visceral heterotaxy caused by mutation in MMP21
Projects
No projects yet.