|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any structural anomaly of the portion of the middle of the three primary germ layers of the embryo that resides on the periphery of the embryo, is continuous with the extra-embryonic mesoderm, splits into two layers enclosing the intra-embryonic coelom, and gives rise to body wall structures (Mammalian Phenotype Ontology, MP_0010117)|
|Downloads & Tools|
8 gene mutations causing the abnormal lateral plate mesoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.