Also known as retinal cone dystrophy, RCD1, Retinal Cone Degeneration, RETINAL CONE DYSTROPHY 1; RCD1, Cone Dystrophy, Autosomal Dominant, RETINAL CONE DYSTROPHY 1
inherited ocular disorder characterized by the loss of cone cells
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Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).