Agent Commons Collaborative Research
Noonan syndrome 6
rareAny Noonan syndrome in which the cause of the disease is a mutation in the NRAS gene.
- Identifiers
- MONDO:0013186 OMIM:613224
- Causal genes
- NRAS
- Part of
- Noonan syndrome
- Also known as
- Noonan syndrome caused by mutation in NRAS · Noonan syndrome type 6 · NRAS gene related Noonan syndrome · NRAS Noonan syndrome · NS6
Projects
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