Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		0.300 GermlineCausalMutation ORPHANET Unexpected genetic heterogeneity for primary ciliary dyskinesia in the Irish Traveller population. 24824133

2015
Entrez Id: 10309
Gene Symbol: CCNO
CCNO
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		0.300 GermlineCausalMutation ORPHANET Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia. 24747639

2014