# amelogenesis imperfecta type 1E

> amelogenesis imperfecta that has material basis in mutation in the gene encoding amelogenin (AMELX)

**Wikidata**: [Q27674802](https://www.wikidata.org/wiki/Q27674802)  
**Source**: https://4ort.xyz/entity/amelogenesis-imperfecta-type-1e


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1)
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)