# acroosteolysis-keloid-like lesions-premature aging syndrome

> human disease

**Wikidata**: [Q55783230](https://www.wikidata.org/wiki/Q55783230)  
**Source**: https://4ort.xyz/entity/acroosteolysis-keloid-like-lesions-premature-aging-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. UniProt
3. A Point Mutation in PDGFRB Causes Autosomal-Dominant Penttinen Syndrome
4. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000113721/MONDO_0011150)