# Fanconi anemia complementation group O

> Fanconi anemia that has material basis in homozygous mutation in the RAD51C gene on chromosome 17q21-q24

**Wikidata**: [Q32147082](https://www.wikidata.org/wiki/Q32147082)  
**Source**: https://4ort.xyz/entity/fanconi-anemia-complementation-group-o


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutation of the RAD51C gene in a Fanconi anemia-like disorder
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)