# primary CD59 deficiency

> human disease

**Wikidata**: [Q55783887](https://www.wikidata.org/wiki/Q55783887)  
**Source**: https://4ort.xyz/entity/primary-cd59-deficiency


## References

1. Monarch Disease Ontology release 2018-06-29
2. Paroxysmal nocturnal hemoglobinuria due to hereditary nucleotide deletion in the HRF20 (CD59) gene
3. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000085063/MONDO_0012858)