# Fanconi anemia complementation group B

> Fanconi anemia that has material basis in mutation in the FANCB gene on chromosome Xp22

**Wikidata**: [Q32147112](https://www.wikidata.org/wiki/Q32147112)  
**Source**: https://4ort.xyz/entity/fanconi-anemia-complementation-group-b-q32147112


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. X-linked inheritance of Fanconi anemia complementation group B
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)