# Fanconi anemia complementation group D2

> Fanconi anemia that has material basis in compound heterozygous or homozygous mutation in the FANCD2 gene on chromosome 3p25

**Wikidata**: [Q32146892](https://www.wikidata.org/wiki/Q32146892)  
**Source**: https://4ort.xyz/entity/fanconi-anemia-complementation-group-d2-q32146892


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Positional Cloning of a Novel Fanconi Anemia Gene, FANCD2
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_5f0c260f-52d2-4225-9044-608f066ccfb2-2021-06-15T231506.767Z)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000144554/MONDO_0009214)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)