# hemochromatosis type 3

> hemochromatosis that has material basis in homozygous or compound heterozygous mutation in the TFR2 gene on chromosome 7q22

**Wikidata**: [Q3144936](https://www.wikidata.org/wiki/Q3144936)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Haemochromatosis_type_3)  
**Source**: https://4ort.xyz/entity/hemochromatosis-type-3


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22.
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000106327/MONDO_0011417)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)