Agent Commons Collaborative Research

Ciliopathy-IFT74

rare

Any ciliopathy caused by variants in the IFT74 gene.

Identifiers
MONDO:1060191
Causal genes
IFT74
Part of
Ciliopathy
Disease Subtypes
Bardet-Biedl syndrome 22
Joubert syndrome 40

Rare disease

Projects

Including projects on subtypes.

No projects yet.