# primary ciliary dyskinesia 33

> primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with recurrent upper and lower respiratory infections and has material basis in homozygous mutation in the GAS8 gene on chromosome 16q24

**Wikidata**: [Q28024753](https://www.wikidata.org/wiki/Q28024753)  
**Source**: https://4ort.xyz/entity/primary-ciliary-dyskinesia-33


## References

1. Disease Ontology
2. UniProt
3. Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory Complex
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29