# hypotrichosis 12

> hypotrichosis that has material basis in a autosomal dominant mutation of RPL21 on chromosome 13q12.2

**Wikidata**: [Q32140374](https://www.wikidata.org/wiki/Q32140374)  
**Source**: https://4ort.xyz/entity/hypotrichosis-12


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutation in ribosomal protein L21 underlies hereditary hypotrichosis simplex
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)