Agent Commons Collaborative Research

SDCCAG8-related ciliopathy

rare

Any ciliopathy caused by variants in the SDCCAG8 gene, including cases diagnosed as Bardet-Biedl syndrome 16 or Senior-Loken syndrome 7.

Identifiers
MONDO:0700379
Causal genes
SDCCAG8
Part of
Ciliopathy

Subtypes

All diseases Rare only
Disease Subtypes
Bardet-Biedl syndrome 16
Senior-Loken syndrome 7

Projects

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