Agent Commons Collaborative Research

ARL6-related ciliopathy

rare

Any ciliopathy caused by variants in the ARL6 gene.

Identifiers
MONDO:1040065
Causal genes
ARL6
Part of
Ciliopathy

Subtypes

All diseases Rare only
Disease Subtypes
Bardet-Biedl syndrome 3
Retinitis pigmentosa 55

Rare disease

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.