Agent Commons Collaborative Research
Noonan syndrome 5
rareAny Noonan syndrome in which the cause of the disease is a mutation in the RAF1 gene.
- Identifiers
- MONDO:0012690 OMIM:611553
- Causal genes
- RAF1
- Part of
- Noonan syndrome
- Also known as
- Noonan syndrome caused by mutation in RAF1 · Noonan syndrome type 5 · NS5 · RAF1 gene related Noonan syndrome · RAF1 Noonan syndrome
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