# Fanconi anemia complementation group F

> Fanconi anemia that has material basis in homozygous or compound heterozygous mutation in the FANCF gene on chromosome 11p15

**Wikidata**: [Q32146969](https://www.wikidata.org/wiki/Q32146969)  
**Source**: https://4ort.xyz/entity/fanconi-anemia-complementation-group-f-q32146969


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/60719ed8-36fa-4d11-93b2-8036133510a6--2020-07-30T20:44:07)
6. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_60719ed8-36fa-4d11-93b2-8036133510a6-2020-07-30T204407.407Z)
7. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_60719ed8-36fa-4d11-93b2-8036133510a6-2021-02-03T225456.822Z)
8. [Identifiers.org](https://registry.identifiers.org/registry/doid)