# amelogenesis imperfecta type 1A

> amelogenesis imperfecta that has material basis in heterozygous mutation in the beta-3 laminin gene (LAMB3) on chromosome 1q32

**Wikidata**: [Q27674799](https://www.wikidata.org/wiki/Q27674799)  
**Source**: https://4ort.xyz/entity/amelogenesis-imperfecta-type-1a


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. LAMB3 Mutations Causing Autosomal-dominant Amelogenesis Imperfecta
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)