|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||absence of the group of neuron cell bodies associated with the eighth cranial nerve during embryogenesis; splits in later development to form the cochlear and vestibular ganglia (Mammalian Phenotype Ontology, MP_0004313)|
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2 gene mutations causing the absent vestibulocochlear ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.