|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any structural anomaly in the fibrovascular mesodermal tissue located between the optic cup and lens vesicle that normally regresses during the development of the vitreous body (Mammalian Phenotype Ontology, MP_0009620)|
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8 gene mutations causing the abnormal primary vitreous morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.