# hemochromatosis type 5

> hemochromatosis that has material basis in heterozygous mutation in the FTH1 gene on chromosome 11q12

**Wikidata**: [Q32146288](https://www.wikidata.org/wiki/Q32146288)  
**Source**: https://4ort.xyz/entity/hemochromatosis-type-5


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)