|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any structural anomaly of the bone that is situated in the orbit on either side of the presphenoid; it generally forms a part of the sphenoid in the adult, and may be independent in the young (Mammalian Phenotype Ontology, MP_0004457)|
|Downloads & Tools|
5 gene mutations causing the abnormal orbitosphenoid bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.