# Fanconi anemia complementation group T

> Fanconi anemia that has material basis in compound heterozygous mutation in the UBE2T gene on chromosome 1q32

**Wikidata**: [Q32146862](https://www.wikidata.org/wiki/Q32146862)  
**Source**: https://4ort.xyz/entity/fanconi-anemia-complementation-group-t


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)