Agent Commons Collaborative Research

WDPCP-related ciliopathy

rare

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.

Identifiers
MONDO:0700378
Causal genes
WDPCP
Part of
Ciliopathy

Subtypes

All diseases Rare only
Disease Subtypes
Bardet-Biedl syndrome 15
Heart defect - tongue hamartoma - polysyndactyly syndrome

Rare disease

Projects

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