agenesis of the corpus callosum Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Absence of the corpus callosum as a result of the failure of the corpus callosum to develop, which can be the result of a failure in any one of the multiple steps of callosal development including cellular proliferation and migration, axonal growth or glial patterning at the midline. (Human Phenotype Ontology, HP_0001274)
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Genes

1 genes associated with the disease agenesis of the corpus callosum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6