# hypotrichosis 2

> hypotrichosis that has material basis in a autosomal dominant mutation of CDSN on chromosome 6p21.33

**Wikidata**: [Q32140239](https://www.wikidata.org/wiki/Q32140239)  
**Source**: https://4ort.xyz/entity/hypotrichosis-2


## References

1. Disease Ontology
2. UniProt
3. Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29