|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||acquired diminution of the size of the midbrain 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_0012507)|
|Downloads & Tools|
1 gene mutations causing the midbrain atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|SMPD1||sphingomyelin phosphodiesterase 1, acid lysosomal|