Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10309
Gene Symbol: CCNO
CCNO 		0.700 Biomarker disease GENOMICS_ENGLAND Risk factors for situs defects and congenital heart disease in primary ciliary dyskinesia. 30166424 2019
Entrez Id: 10309
Gene Symbol: CCNO
CCNO 		0.700 GeneticVariation disease UNIPROT Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis. 26777464 2016
Entrez Id: 10309
Gene Symbol: CCNO
CCNO 		0.700 GeneticVariation disease UNIPROT Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia. 24747639 2014
Entrez Id: 10309
Gene Symbol: CCNO
CCNO 		0.700 Biomarker disease GENOMICS_ENGLAND Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia. 24747639 2014
Entrez Id: 10309
Gene Symbol: CCNO
CCNO 		0.700 Biomarker disease CTD_human
Entrez Id: 10309
Gene Symbol: CCNO
CCNO 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 10309
Gene Symbol: CCNO
CCNO 		0.700 CausalMutation disease CLINVAR