# Noonan syndrome 5

> Noonan syndrome that has material basis in mutation in the RAF1 gene

**Wikidata**: [Q26492793](https://www.wikidata.org/wiki/Q26492793)  
**Source**: https://4ort.xyz/entity/noonan-syndrome-5


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)