# nemaline myopathy 4

> nemaline myopathy that has material basis in heterozygous mutation in the TPM2 gene on chromosome 9p13

**Wikidata**: [Q32144895](https://www.wikidata.org/wiki/Q32144895)  
**Source**: https://4ort.xyz/entity/nemaline-myopathy-4


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)