# primary ciliary dyskinesia 6

> primary ciliary dyskinesia that is characterized by partial outer dynein arm defect and has material basis in mutation in the TXNDC3 gene on the chromosome 7p14.1

**Wikidata**: [Q28024738](https://www.wikidata.org/wiki/Q28024738)  
**Source**: https://4ort.xyz/entity/primary-ciliary-dyskinesia-6


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)