# Fanconi anemia complementation group V

> Fanconi anemia that has material basis in homozygous mutation in the MAD2L2 gene on chromosome 1p36

**Wikidata**: [Q32146849](https://www.wikidata.org/wiki/Q32146849)  
**Source**: https://4ort.xyz/entity/fanconi-anemia-complementation-group-v


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Biallelic inactivation of REV7 is associated with Fanconi anemia
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)