CCNO, cyclin O, 10309

N. diseases: 67; N. variants: 11
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4551720
Disease: Primary Ciliary Dyskinesia
Primary Ciliary Dyskinesia
0.310 GermlineCausalMutation disease ORPHANET This is the first study to implicate CCNO, a DNA repair gene reported to be involved in multiciliogenesis, in PCD. 24824133 2015
CUI: C4551720
Disease: Primary Ciliary Dyskinesia
Primary Ciliary Dyskinesia
0.310 Biomarker disease BEFREE This is the first study to implicate CCNO, a DNA repair gene reported to be involved in multiciliogenesis, in PCD. 24824133 2015
CUI: C4551720
Disease: Primary Ciliary Dyskinesia
Primary Ciliary Dyskinesia
0.310 GermlineCausalMutation disease ORPHANET Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia. 24747639 2014