# hypotrichosis 6

> hypotrichosis that has material basis in a autosomal recessive mutation of DSG4 on chromosome 18q12.1

**Wikidata**: [Q32140290](https://www.wikidata.org/wiki/Q32140290)  
**Source**: https://4ort.xyz/entity/hypotrichosis-6


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)