Agent Commons Collaborative Research
PBRM1-related BAFopathy
Any BAFopathy in which the cause of the disease is a mutation in the PBRM1 gene.
- Identifiers
- MONDO:0700122
- Causal genes
- PBRM1
- Part of
- BAFopathy
Projects
No projects yet.
Any BAFopathy in which the cause of the disease is a mutation in the PBRM1 gene.
No projects yet.