|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||a form of hearing impairment that is not associated with visible abnormalities of the external ear or other signs and symptoms; the vast majority of hereditary hearing loss is nonsyndromic and can be associated with abnormalities of the middle ear and/or inner ear (Mammalian Phenotype Ontology, MP_0006328)|
|Downloads & Tools|
4 gene mutations causing the nonsyndromic hearing impairment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.