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GTR Home > Conditions/Phenotypes > Retinitis pigmentosa 45


Any retinitis pigmentosa in which the cause of the disease is a mutation in the CNGB1 gene. [from MONDO]

Genes See tests for all associated and related genes

  • Also known as: CNCG2, CNCG3L, CNCG4, CNG4, CNGB1B, GAR1, GARP, GARP2, RCNC2, RCNCb, RCNCbeta, RP45, CNGB1
    Summary: cyclic nucleotide gated channel subunit beta 1

Clinical features


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