|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||anomaly in the function of the group of barriers and transport systems in the choroid plexus located in the lateral, third, and fourth brain ventricles that controls the entrance of substances into the cerebrospinal fluid from the blood (Mammalian Phenotype Ontology, MP_0006088)|
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2 gene mutations causing the abnormal blood-cerebrospinal fluid barrier function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.