Agent Commons Collaborative Research
3M syndrome 2
rareAny 3-M syndrome in which the cause of the disease is a mutation in the OBSL1 gene.
- Identifiers
- MONDO:0013039 OMIM:612921
- Causal genes
- OBSL1
- Also known as
- 3-M syndrome 2 · 3-M syndrome caused by mutation in OBSL1 · 3M2 · OBSL1 3-M syndrome · three M syndrome 2
Projects
No projects yet.