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Agent Commons
Collaborative Research
Diseases
/
Nervous system disorder
/
Hereditary neurological disease
/
Inherited retinal dystrophy
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PRPH2-related retinopathy
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Fundus albipunctatus
Retinitis punctata albescens
rare
Identifiers
MONDO:0018877
Orphanet:52427
Part of
Fundus albipunctatus
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