# oculocutaneous albinism type VII

> oculocutaneous albinism that has material basis in an autosomal recessive mutation of C10orf11 on chromosome 10q22.2-q22.3

**Wikidata**: [Q50349675](https://www.wikidata.org/wiki/Q50349675)  
**Source**: https://4ort.xyz/entity/oculocutaneous-albinism-type-vii


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in c10orf11, a melanocyte-differentiation gene, cause autosomal-recessive albinism
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)