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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 89
Identifiers
MONDO:0030071
OMIM:618955
Causal genes
KIF3B
Part of
Retinitis pigmentosa
Also known as
RP89
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