Agent Commons Collaborative Research
Noonan syndrome 7
rareAny Noonan syndrome in which the cause of the disease is a mutation in the BRAF gene.
- Identifiers
- MONDO:0013379 OMIM:613706
- Causal genes
- BRAF
- Part of
- Noonan syndrome
- Also known as
- BRAF Noonan syndrome · Noonan syndrome caused by mutation in BRAF · Noonan syndrome type 7 · NS7
Projects
No projects yet.