# Usher syndrome type 1G

> Usher syndrome type 1 that has material basis in caused by homozygous or compound heterozygous mutation in the USH1G gene on chromosome 17q25

**Wikidata**: [Q32143575](https://www.wikidata.org/wiki/Q32143575)  
**Source**: https://4ort.xyz/entity/usher-syndrome-type-1g


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)