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Summary Literature (0)
MIM:610024 - RETINAL CONE DYSTROPHY 3A; RCD3A

Xenbase Genes: pde6h

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012398 - retinal cone dystrophy 3A
MONDO:0018852 - achromatopsia

Disease Ontology (DO):
DOID:0050795 - cone dystrophy
DOID:0081025 - retinal cone dystrophy 3A