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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
Macular dystrophy with or without cone dysfunction
rare
Identifiers
MONDO:0958326
OMIM:620762
Causal genes
SAMD7
Part of
Hereditary macular dystrophy
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