# hypotrichosis 11

> hypotrichosis that has material basis in a autosomal dominant mutation of SNRPE on chromosome 1q32.1

**Wikidata**: [Q32140359](https://www.wikidata.org/wiki/Q32140359)  
**Source**: https://4ort.xyz/entity/hypotrichosis-11


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)