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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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Cone-rod dystrophy
Cone-rod dystrophy 22
rare
Identifiers
MONDO:0030440
OMIM:619531
Causal genes
TLCD3B
Part of
Cone-rod dystrophy
Also known as
CORD22
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