|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any structural anomaly of the nonmotile primary cilium that is found at the apical surface of inner hair cells (Mammalian Phenotype Ontology, MP_0011061)|
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5 gene mutations causing the abnormal inner hair cell kinocilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.