# Noonan syndrome 6

> Noonan syndrome that has material basis in heterozygous mutation in the NRAS gene on chromosome 1p13

**Wikidata**: [Q26492794](https://www.wikidata.org/wiki/Q26492794)  
**Source**: https://4ort.xyz/entity/noonan-syndrome-6


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. A restricted spectrum of NRAS mutations causes Noonan syndrome
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)