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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Cone-rod dystrophy and hearing loss
Cone-rod dystrophy and hearing loss 2
Identifiers
MONDO:0020780
OMIM:618358
Causal genes
CEP250
Part of
Cone-rod dystrophy and hearing loss
Also known as
CRDHL2
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