|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||anomaly in the organization of the various cell types within the organ of Corti into a set number of distinct rows (Mammalian Phenotype Ontology, MP_0006331)|
|Downloads & Tools|
2 gene mutations causing the abnormal patterning of the organ of corti phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.