# nemaline myopathy 6

> human disease

**Wikidata**: [Q32144933](https://www.wikidata.org/wiki/Q32144933)  
**Source**: https://4ort.xyz/entity/nemaline-myopathy-6


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with cores
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000234438/MONDO_0012237)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)