# hypertrophic cardiomyopathy 20

> hypertrophic cardiomyopathy that hhas material basis in heterozygous mutation in the NEXN gene on chromosome 1p31.1

**Wikidata**: [Q27674939](https://www.wikidata.org/wiki/Q27674939)  
**Source**: https://4ort.xyz/entity/hypertrophic-cardiomyopathy-20


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000162614/MONDO_0013477)
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)