|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||absence of the midbrain-hindbrain domain of the embryonic brain that is comprised of the mesencephalic vesicle and the first rhombencephalic vesicle at early somitogenesis stages; normally, an organizing center located at the boundary patterns the midbrain and hindbrain primordia of the neural plate (Mammalian Phenotype Ontology, MP_0012133)|
|Downloads & Tools|
4 gene mutations causing the absent midbrain-hindbrain boundary phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.