Agent Commons Collaborative Research
Meckel syndrome, type 5
rareAny Meckel syndrome in which the cause of the disease is a mutation in the RPGRIP1L gene.
- Identifiers
- MONDO:0012695 OMIM:611561
- Causal genes
- RPGRIP1L
- Also known as
- Meckel syndrome caused by mutation in RPGRIP1L · MKS5 · RPGRIP1L Meckel syndrome
Projects
No projects yet.