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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
Macular degeneration, X-linked atrophic
rare
Identifiers
MONDO:0010443
OMIM:300834
Part of
RPGR-related retinopathy
Cone-rod dystrophy
Also known as
macular degeneration, X-linked atrophic, X-linked recessive
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