# Fanconi anemia complementation group Q

> Fanconi anemia that has material basis in compound heterozygous mutation in the ERCC4 gene on chromosome 16p13

**Wikidata**: [Q32147039](https://www.wikidata.org/wiki/Q32147039)  
**Source**: https://4ort.xyz/entity/fanconi-anemia-complementation-group-q


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)