Acrocallosal Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
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4 genes/proteins associated with the disease Acrocallosal Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
KIF7 kinesin family member 7 2.88009
ACLS acrocallosal syndrome 2.88009
FOXG1 forkhead box G1 2.88009
GLI3 GLI family zinc finger 3 2.88009