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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 79
rare
Identifiers
MONDO:0044320
OMIM:617460
Causal genes
HK1
Part of
Retinitis pigmentosa
Also known as
RP79
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