|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any structural anomaly of the region of a cerebellar lobule that resides in the central section of the cerebellum between the two hemispheres; in humans, vermis lobule regions may be nearly continuous with the cerebellar hemisphere lobules dorsally but are separated by deeper longitudinal fissues in the ventral regions; in mammals, the vermis portion of the cerebellum has a foliation pattern along the AP axis that is distinct from the lateral cerebellar hemispheres (Mammalian Phenotype Ontology, MP_0009957)|
|Downloads & Tools|
6 gene mutations causing the abnormal cerebellum vermis lobule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.