# Usher syndrome type 1F

> Usher syndrome type 1 that has material basis in caused by homozygous or compound heterozygous mutation in the PCDH15 gene on chromosome 10q

**Wikidata**: [Q32143548](https://www.wikidata.org/wiki/Q32143548)  
**Source**: https://4ort.xyz/entity/usher-syndrome-type-1f


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)