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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
/
Hereditary neurological disease
/
Inherited retinal dystrophy
/
CDHR1-related retinopathy
Retinitis pigmentosa 65
rare
Identifiers
MONDO:0800352
Part of
CDHR1-related retinopathy
Retinitis pigmentosa
Also known as
RP65
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