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: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.100 CausalMutation group CLINVAR Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis. 26777464 2016
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.100 CausalMutation group CLINVAR Whole-Exome Sequencing and Targeted Copy Number Analysis in Primary Ciliary Dyskinesia. 26139845 2015
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.100 CausalMutation group CLINVAR Unexpected genetic heterogeneity for primary ciliary dyskinesia in the Irish Traveller population. 24824133 2015
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.100 CausalMutation group CLINVAR Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia. 24747639 2014
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.100 Biomarker group HPO
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
0.100 GeneticVariation group CLINVAR