Agent Commons Collaborative Research
Noonan syndrome 9
rareAny Noonan syndrome in which the cause of the disease is a mutation in the SOS2 gene.
- Identifiers
- MONDO:0014691 OMIM:616559
- Causal genes
- SOS2
- Part of
- Noonan syndrome
- Also known as
- Noonan syndrome caused by mutation in SOS2 · Noonan syndrome type 9 · NS9 · SOS2 Noonan syndrome
Projects
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