# Fanconi anemia complementation group R

> Fanconi anemia that has material basis in heterozygous mutation in the RAD51 gene on chromosome 15q15

**Wikidata**: [Q32147000](https://www.wikidata.org/wiki/Q32147000)  
**Source**: https://4ort.xyz/entity/fanconi-anemia-complementation-group-r


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)