|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any structural anomaly of the opening on the medial wall of the middle ear leading into the cochlea, closed in life by the secondary tympanic membrane; serves to regulate fluid pressure in the inner ear (Mammalian Phenotype Ontology, MP_0004480)|
|Downloads & Tools|
4 gene mutations causing the abnormal round window morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.