# basal laminar drusen

> retinal drusen characterized by yellow-white deposits (drusen) that accumulate beneath the retinal pigment epithelium on Bruch membrane and that has material basis in mutations in the CFH gene on chromosome 1q31.3

**Wikidata**: [Q28065549](https://www.wikidata.org/wiki/Q28065549)  
**Source**: https://4ort.xyz/entity/basal-laminar-drusen


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Basal laminar drusen caused by compound heterozygous variants in the CFH gene
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)