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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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ELOVL4-related maculopathy
Stargardt disease 3
rare
Identifiers
MONDO:0010819
OMIM:600110
Part of
ELOVL4-related maculopathy
Stargardt disease
Also known as
Stargardt disease type 3 · STGD3
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