# primary ciliary dyskinesia 21

> primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with a missing Nexin link, infantile onset of chronic sinopulmonary infections, and has material basis in homozygous mutation in the DRC1 gene on chromosome 2p23

**Wikidata**: [Q28024727](https://www.wikidata.org/wiki/Q28024727)  
**Source**: https://4ort.xyz/entity/primary-ciliary-dyskinesia-21


## References

1. Disease Ontology
2. UniProt
3. The nexin-dynein regulatory complex subunit DRC1 is essential for motile cilia function in algae and humans
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29