# Usher syndrome type 1D

> Usher syndrome type 1 that has material basis in homozygous or compound heterozygous mutation in the CDH23 gene on chromosome 10q22

**Wikidata**: [Q32143535](https://www.wikidata.org/wiki/Q32143535)  
**Source**: https://4ort.xyz/entity/usher-syndrome-type-1d


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans
5. Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)