|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A structural anomaly of the two central microtubules of motile cilia with a 9+2 microtubuluar configuration. (Human Phenotype Ontology, HP_0012260)|
|Downloads & Tools|
2 genes associated with the abnormal central microtubular pair morphology of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.