Motile ciliopathy with hydrocephalus and randomization of left/right body asymmetry

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
motile ciliopathy with hydrocephalus and randomization of left/right body asymmetry
MONDO_0032874
FOXJ1 Unknown
31630787
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Motile ciliopathy with hydrocephalus and randomization of left/right body asymmetry.
5 View disease cluster →
Ciliary dyskinesia, primary, 43 1 shared geneFOXJ1 Related via 1 shared gene including FOXJ1. Allergic rhinitis 1 shared geneFOXJ1 Related via 1 shared gene including FOXJ1. Hydrocephalus 1 shared geneFOXJ1 Related via 1 shared gene including FOXJ1. Ciliary dyskinesia 1 shared geneFOXJ1 Related via 1 shared gene including FOXJ1. Tetralogy of fallot 1 shared geneFOXJ1 Related via 1 shared gene including FOXJ1.