|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||acquired diminution of the size of the second cranial nerve which is responsible for conveying visual information from the retina to the brain, associated with wasting as from death and reabsorbtion of cells, diminished cellular proliferation, decreased cellular volume, pressure, ischemia, malnutrition, reduced function or malfunction, or hormonal changes (Mammalian Phenotype Ontology, MP_0001059)|
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6 gene mutations causing the optic nerve atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.