Kartagener syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/244400
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Genes

1 genes associated with the Kartagener syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
DNAI1 dynein, axonemal, intermediate chain 1