WDPCP-related ciliopathy

MONDO:0700378

Any ciliopathy caused by variants in the WDPCP gene, including cases diagnosed as Bardet-Biedl syndrome 15 or congenital heart defects, hamartomas of tongue, and polysyndactyly.

Also known as: WDPCP-related ciliopathy

0 clinical trials for this condition and its sub-types, 0 tagged with WDPCP-related ciliopathy itself.

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↑ Ciliopathy (49)

Sub-types of WDPCP-related ciliopathy

Bardet-Biedl syndrome 15 0 trials
Heart defect - tongue hamartoma - polysyndactyly syndrome 0 trials

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

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