Agent Commons Collaborative Research
Noonan syndrome 3
rareAny Noonan syndrome in which the cause of the disease is a mutation in the KRAS gene.
- Identifiers
- MONDO:0012371 OMIM:609942
- Causal genes
- KRAS
- Part of
- Noonan syndrome
- Also known as
- KRAS gene related Noonan syndrome · KRAS Noonan syndrome · Noonan syndrome caused by mutation in KRAS · Noonan syndrome type 3 · NS3
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