Joubert syndrome with cranio-facial and skeletal defects

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Subtype of: Joubert syndrome
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Joubert syndrome with cranio-facial and skeletal defects
MONDO_0033309
SUFU Unknown
28965847
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Joubert syndrome with cranio-facial and skeletal defects.
5 View disease cluster →
Joubert and congenital ocular motor apraxia 1 shared geneSUFU Related via 1 shared gene including SUFU. Familial meningioma 1 shared geneSUFU Related via 1 shared gene including SUFU. Gorlin syndrome 1 shared geneSUFU Related via 1 shared gene including SUFU. Basal cell nevus syndrome 1 shared geneSUFU Related via 1 shared gene including SUFU. Mixed neuronal-glial tumor 1 shared geneSUFU Related via 1 shared gene including SUFU.