# hypotrichosis 8

> hypotrichosis has material basis in a autosomal recessive mutation of LPAR6 on chromosome 13q14.2

**Wikidata**: [Q32140317](https://www.wikidata.org/wiki/Q32140317)  
**Source**: https://4ort.xyz/entity/hypotrichosis-8


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hair
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)