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
CFAP221 Causal — ClinGen —
CFAP57 Causal — ClinGen —
DAW1 Causal — ClinGen —
DNAH1 Causal — ClinGen
DNAH7 Causal — ClinGen
SPEF2 Causal — ClinGen —
All9 Causal6 Unknown3
Related Diseases Diseases that share the most curated genes with primary ciliary dyskinesia.
5 View disease cluster →
Congenital impairment of spermatozoa motility 3 shared genesSPEF2, CFAP43, DNAH1 Related via 3 shared genes including SPEF2, CFAP43, DNAH1. spermatogenic failure 56 1 shared geneDNAH10 Related via 1 shared gene including DNAH10. Young syndrome 1 shared geneCFAP221 Related via 1 shared gene including CFAP221. spermatogenic failure 19 1 shared geneCFAP43 Related via 1 shared gene including CFAP43. spermatogenic failure 18 1 shared geneDNAH1 Related via 1 shared gene including DNAH1.