# amelogenesis imperfecta type 2A1

> amelogenesis imperfecta that has material basis in homozygous mutation in the kallikrein-4 gene (KLK4) on chromosome 19q13

**Wikidata**: [Q27674801](https://www.wikidata.org/wiki/Q27674801)  
**Source**: https://4ort.xyz/entity/amelogenesis-imperfecta-type-2a1


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)