# Fanconi anemia complementation group I

> Fanconi anemia that has material basis in homozygous or compound heterozygous mutation in the FANCI gene on chromosome 15q26

**Wikidata**: [Q32147011](https://www.wikidata.org/wiki/Q32147011)  
**Source**: https://4ort.xyz/entity/fanconi-anemia-complementation-group-i-q32147011


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Identification of the Fanconi Anemia Complementation Group I Gene, FANCI
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_a103db2f-a8b3-403b-993a-ac4215c118df-2021-06-15T233841.081Z)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000140525/MONDO_0012186)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)