Joubert and congenital ocular motor apraxia

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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Joubert and congenital ocular motor apraxia
MONDO_0700092
SUFU Unknown
33024317 34675124
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Joubert and congenital ocular motor apraxia.
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Joubert syndrome with cranio-facial and skeletal defects 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.