|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any structural anomaly in the small artery that passes through the ring of the stapes; while the stapedial artery is a temporary artery thought to disappear at late embryonic stage in humans, the mouse stapedial artery is complete by E13 and persists into adulthood (Mammalian Phenotype Ontology, MP_0004665)|
|Downloads & Tools|
6 gene mutations causing the abnormal stapedial artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.