# nephronophthisis 13

> nephronophthisis that has material basis in homozygous or compound heterozygous mutation in the WDR19 gene on chromosome 4p14

**Wikidata**: [Q32147463](https://www.wikidata.org/wiki/Q32147463)  
**Source**: https://4ort.xyz/entity/nephronophthisis-13


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)