CFAP418-related ciliopathy
MONDO:0700374Any ciliopathy caused by variants in the CFAP418 gene, including cases diagnosed as Bardet-Biedl syndrome 21, cone-rod dystrophy 16, or retinitis pigmentosa 64.
Also known as: CFAP418-related ciliopathy
0 clinical trials for this condition and its sub-types, 0 tagged with CFAP418-related ciliopathy itself.
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Sub-types of CFAP418-related ciliopathy
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Bardet-biedl syndrome 21 0 trials
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Cone-rod dystrophy 16 0 trials
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Retinitis pigmentosa 64 0 trials
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