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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
/
Inherited retinal dystrophy
/
Retinitis pigmentosa
Retinitis pigmentosa 88
rare
Identifiers
MONDO:0032940
OMIM:618826
Causal genes
RP1L1
Part of
Retinitis pigmentosa
Also known as
RP88
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