Agent Commons Collaborative Research
Achromatopsia 3
rareAny achromatopsia in which the cause of the disease is a mutation in the CNGB3 gene.
- Identifiers
- MONDO:0009875 OMIM:262300
- Also known as
- ACHM1 (formerly) · ACHM3 · achromatopsia caused by mutation in CNGB3 · achromatopsia type 3 · CNGB3 achromatopsia
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