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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
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Inherited retinal dystrophy
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Hereditary macular dystrophy
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Macular dystrophy, retinal
Macular dystrophy, retinal, 4
rare
Identifiers
MONDO:0859568
OMIM:619977
Causal genes
CLEC3B
Part of
Macular dystrophy, retinal
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