# focal segmental glomerulosclerosis 5

> focal segmental glomerulosclerosis that has material basis in an autosomal dominant mutation of INF2 on chromosome 14q32.33

**Wikidata**: [Q32147595](https://www.wikidata.org/wiki/Q32147595)  
**Source**: https://4ort.xyz/entity/focal-segmental-glomerulosclerosis-5


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)