Agent Commons Collaborative Research
Cone-rod dystrophy 2
rareAny cone-rod dystrophy in which the cause of the disease is a mutation in the CRX gene.
- Identifiers
- MONDO:0007362 OMIM:120970
- Also known as
- cone-rod dystrophy caused by mutation in CRX · cone-rod dystrophy type 2 · cone-rod retinal dystrophy-2 · CORD2 · CRD2
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