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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
/
Hereditary neurological disease
/
Inherited retinal dystrophy
/
Retinitis pigmentosa
Retinitis pigmentosa 78
rare
Identifiers
MONDO:0044314
OMIM:617433
Causal genes
ARHGEF18
Part of
Retinitis pigmentosa
Also known as
RP78
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