|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any structural anomaly of the crescent-shaped, ventrally located fold of the embryonic disc at the future cephalic end of the developing embryo; it constitutes the first body fold, and initiates brain, foregut and heart development (Mammalian Phenotype Ontology, MP_0011257)|
|Downloads & Tools|
8 gene mutations causing the abnormal head fold morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.