# Fanconi anemia complementation group C

> Fanconi anemia that has material basis in homozygous or compound heterozygous mutation in the FANCC gene on chromosome 9q22

**Wikidata**: [Q32146953](https://www.wikidata.org/wiki/Q32146953)  
**Source**: https://4ort.xyz/entity/fanconi-anemia-complementation-group-c-q32146953


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Cloning of cDNAs for Fanconi's anaemia by functional complementation
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/cf4881c3-15b3-4e10-bd24-2da80433863b--2019-04-19T16:00:00)
6. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_cf4881c3-15b3-4e10-bd24-2da80433863b-2018-12-21T152145.877Z)
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000158169/MONDO_0009213)
8. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)