|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||A primary ciliary dyskinesia that results from dysfunction of the cilia during embryologic development and is characterized by the triad of sinusitis, bronchiectasis and situs inversus with dextrocardia. (Human Disease Ontology, DOID_0050144)|
|Downloads & Tools|
1 genes associated with the Kartagener syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|DNAI1||dynein, axonemal, intermediate chain 1|