Frontoparietal Cortical Dysplasia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
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 https://www.disgenet.org/browser/0/1/0/C4024959
Similar Terms
Downloads & Tools

Genes

1 genes associated with the disease Frontoparietal Cortical Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
TUBB2B tubulin, beta 2B class IIb