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CFAP418-related ciliopathy

MONDO:0700374

Any 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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↑ Ciliopathy (49)

Sub-types of CFAP418-related ciliopathy

Bardet-biedl syndrome 21 0 trials
Cone-rod dystrophy 16 0 trials
Retinitis pigmentosa 64 0 trials

Including sub-types (0) Tagged with CFAP418-related ciliopathy (0)

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