# nephronophthisis 7

> nephronophthisis that has material basis in homozygous mutation in the GLIS2 gene on chromosome 16p13

**Wikidata**: [Q32147386](https://www.wikidata.org/wiki/Q32147386)  
**Source**: https://4ort.xyz/entity/nephronophthisis-7


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)