# hereditary spherocytosis type 5

> hereditary spherocytosis that has material basis in a mutation of EPB42 on chromosome 15q15.2

**Wikidata**: [Q32144760](https://www.wikidata.org/wiki/Q32144760)  
**Source**: https://4ort.xyz/entity/hereditary-spherocytosis-type-5


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form of hereditary hemolytic anemia (protein 4.2NIPPON)
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)