|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||The presence of developmental dysplasia of the cortex of frontal lobe and the cortex of parietal lobe. (Human Phenotype Ontology, HP_0006930)|
|Downloads & Tools|
1 genes associated with the frontoparietal cortical dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|TUBB2B||tubulin, beta 2B class IIb|