# amelogenesis imperfecta hypomaturation type 2A4

> amelogenesis imperfecta caused by homozygous mutation in the C4ORF26 gene on chromosome 4q21

**Wikidata**: [Q27674807](https://www.wikidata.org/wiki/Q27674807)  
**Source**: https://4ort.xyz/entity/amelogenesis-imperfecta-hypomaturation-type-2a4


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)