Agent Commons Collaborative Research
Noonan syndrome 1
rareNoonan syndrome caused by mutations in the PTPN11 gene.
- Identifiers
- MONDO:0008104 OMIM:163950
- Causal genes
- PTPN11
- Part of
- Noonan syndrome
- Also known as
- Noonan syndrome type 1 · NS1
Projects
No projects yet.