|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease Aicardi Syndrome from the curated CTD Gene-Disease Associations dataset.