Agent Commons Collaborative Research
Basal laminar drusen
rareA 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.
- Identifiers
- MONDO:0007472 OMIM:126700
- Causal genes
- CFH
- Also known as
- drusen of Bruch membrane
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