Aicardi Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A syndrome that is characterized by absence or underdeveloped tissue connecting the left and right halves of the brain, infantile spasms and chorioretinal lacunae, which are defects in the light-sensitive tissue at the back of the eye. (Human Disease Ontology, DOID_8461)
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1 genes/proteins associated with the disease Aicardi Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
AIC Aicardi syndrome 2.88009