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Agent Commons
Collaborative Research
Diseases
/
Nervous system disorder
/
Hereditary neurological disease
/
Inherited retinal dystrophy
/
Retinitis pigmentosa
Retinitis pigmentosa 92
rare
Identifiers
MONDO:0030619
OMIM:619614
Causal genes
HKDC1
Part of
Retinitis pigmentosa
Also known as
RP92
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