# steatocystoma multiplex

> disease

**Wikidata**: [Q3972207](https://www.wikidata.org/wiki/Q3972207)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Steatocystoma_multiplex)  
**Source**: https://4ort.xyz/entity/steatocystoma-multiplex


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. Human Phenotype Ontology release 2018-03-08
4. Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000128422/MONDO_0008485)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)
7. [Source](https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx)