|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A syndrome that is an autosomal recessive disorder, which is characterized by corpus callosum agenesis, polydactyly, multiple dysmorphic features, motor and mental retardation. (Human Disease Ontology, DOID_9250)|
|Downloads & Tools|
4 genes/proteins associated with the disease Acrocallosal Syndrome from the curated CTD Gene-Disease Associations dataset.