# hereditary pyropoikilocytosis

> autosomal recessive inherited severe hemolytic anemia. It is a subtype of hereditary elliptocytosis and is characterized by partial spectrin deficiency

**Wikidata**: [Q5737872](https://www.wikidata.org/wiki/Q5737872)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Hereditary_pyropoikilocytosis)  
**Source**: https://4ort.xyz/entity/hereditary-pyropoikilocytosis


## References

1. Monarch Disease Ontology release 2018-06-29
2. Human Phenotype Ontology release 2018-03-08
3. Source
4. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000163554/MONDO_0009948)