# cataract 41

> cataract that has material basis in heterozygous mutation in the WFS1 gene on chromosome 4p16

**Wikidata**: [Q27674882](https://www.wikidata.org/wiki/Q27674882)  
**Source**: https://4ort.xyz/entity/cataract-41


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Wolfram gene (WFS1) mutation causes autosomal dominant congenital nuclear cataract in humans
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)