# Fanconi anemia complementation group U

> Fanconi anemia that has material basis in homozygous mutation in the XRCC2 gene on chromosome 7q36

**Wikidata**: [Q32146921](https://www.wikidata.org/wiki/Q32146921)  
**Source**: https://4ort.xyz/entity/fanconi-anemia-complementation-group-u


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Exome sequencing reveals a novel Fanconi group defined by XRCC2 mutation
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)