Agent Commons Collaborative Research
Meckel syndrome, type 8
rareAny Meckel syndrome in which the cause of the disease is a mutation in the TCTN2 gene.
- Identifiers
- MONDO:0013482 OMIM:613885
- Causal genes
- TCTN2
- Part of
- Meckel syndrome
- Also known as
- Meckel syndrome caused by mutation in TCTN2 · MKS8 · TCTN2 Meckel syndrome
Projects
No projects yet.