Primary ciliary dyskinesia 32

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Subtype of: Primary ciliary dyskinesia
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
primary ciliary dyskinesia 32
EFO_1001352
RSPH3 Causal
26073779
ClinGen, Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Primary ciliary dyskinesia 32.
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Congenital nasopharyngeal atresia 1 shared geneRSPH3 Related via 1 shared gene including RSPH3. Ciliary dyskinesia 1 shared geneRSPH3 Related via 1 shared gene including RSPH3. Systemic lupus erythematosus 1 shared geneRSPH3 Related via 1 shared gene including RSPH3. Attention deficit hyperactivity disorder 1 shared geneRSPH3 Related via 1 shared gene including RSPH3.