# Usher syndrome type 1J

> Usher syndrome type 1 that has material basis in caused by homozygous mutation in the CIB2 gene on chromosome 15q24

**Wikidata**: [Q32143604](https://www.wikidata.org/wiki/Q32143604)  
**Source**: https://4ort.xyz/entity/usher-syndrome-type-1j


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)