Asperger Syndrome Gene Set

Dataset	CTD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	An autism spectrum disorder that is characterized by significant difficulties in social interaction, along with restricted and repetitive patterns of behavior and interests. It differs from other autism spectrum disorders by its relative preservation of linguistic and cognitive development. (Human Disease Ontology, DOID_0050432)
External Link	http://ctdbase.org/detail.go?type=disease&acc=MESH:D020817
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Genes

6 genes/proteins associated with the disease Asperger Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol	Name	Standardized Value
ASPG2	Asperger syndrome, susceptibility to, 2	2.88009
ASPG3	Asperger syndrome, susceptibility to, 3	2.88009
ASPG4	Asperger syndrome, susceptibility to, 4	2.88009
DISC1	disrupted in schizophrenia 1	2.88009
ASPG1	Asperger syndrome, susceptibility to, 1	2.88009
SLC6A4	solute carrier family 6 (neurotransmitter transporter), member 4	2.88009