# nemaline myopathy 11

> nemaline myopathy characterized by onset of slowly progressive muscle weakness in the first decade of life that has material basis in homozygous or compound heterozygous mutation in the MYPN gene on chromosome 10q21

**Wikidata**: [Q32144908](https://www.wikidata.org/wiki/Q32144908)  
**Source**: https://4ort.xyz/entity/nemaline-myopathy-11


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Biallelic Mutations in MYPN, Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/6aeb67cc-c960-4511-a708-b0acadb34588--2020-06-17T19:46:36)
6. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_6aeb67cc-c960-4511-a708-b0acadb34588-2020-06-17T194636.472Z)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)