Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 115948
Gene Symbol: CCDC151
CCDC151
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		0.540 GermlineCausalMutation ORPHANET CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation. 25192045

2014