# hypotrichosis 13

> hypotrichosis that has material basis in a autosomal dominant mutation of KRT71 on chromosome 12q13.13

**Wikidata**: [Q32140386](https://www.wikidata.org/wiki/Q32140386)  
**Source**: https://4ort.xyz/entity/hypotrichosis-13


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. A missense mutation within the helix initiation motif of the keratin K71 gene underlies autosomal dominant woolly hair/hypotrichosis
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)