frontoparietal cortical dysplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of developmental dysplasia of the cortex of frontal lobe and the cortex of parietal lobe. (Human Phenotype Ontology, HP_0006930)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006930
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Genes

1 genes associated with the frontoparietal cortical dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
TUBB2B tubulin, beta 2B class IIb