# Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

> human disease

**Wikidata**: [Q55784010](https://www.wikidata.org/wiki/Q55784010)  
**Source**: https://4ort.xyz/entity/noonan-syndrome-like-disorder-with-juvenile-myelomonocytic-leukemia


## References

1. Monarch Disease Ontology release 2018-06-29
2. UniProt
3. Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype.
4. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/4a1a76fd-7e23-44a7-b2fc-4495bc5d5ee6--2019-04-29T16:00:00)
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_4a1a76fd-7e23-44a7-b2fc-4495bc5d5ee6-2019-04-29T160000.000Z)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000110395/MONDO_0013308)
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000110395/Orphanet_363972)
8. UMLS 2023