# hypertrophic cardiomyopathy 10

> hypertrophic cardiomyopathy that has material basis in mutation in the MYL2 gene

**Wikidata**: [Q27674928](https://www.wikidata.org/wiki/Q27674928)  
**Source**: https://4ort.xyz/entity/hypertrophic-cardiomyopathy-10


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/8768)
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGCIEX:assertion_8768)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000111245/MONDO_0012112)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)