# cataract 45

> cataract that has material basis in homozygous mutation in the SIPA1L3 gene on chromosome 19q13

**Wikidata**: [Q27429764](https://www.wikidata.org/wiki/Q27429764)  
**Source**: https://4ort.xyz/entity/cataract-45


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. SIPA1L3 identified by linkage analysis and whole-exome sequencing as a novel gene for autosomal recessive congenital cataract.
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)