# cataract 17 multiple types

> cataract that has material basis in heterozygous or homozygous mutation in the beta-B1 crystallin gene (CRYBB1) on chromosome 22q12

**Wikidata**: [Q27674909](https://www.wikidata.org/wiki/Q27674909)  
**Source**: https://4ort.xyz/entity/cataract-17-multiple-types


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. A nonsense mutation in CRYBB1 associated with autosomal dominant cataract linked to human chromosome 22q
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)