neurobehavioral manifestations Gene Set

Dataset	GAD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	Signs and symptoms of higher cortical dysfunction caused by organic conditions. These include certain behavioral alterations and impairments of skills involved in the acquisition, processing, and utilization of knowledge or information. (Experimental Factor Ontology, EFO_0004364)
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Genes

9 genes associated with the disease neurobehavioral manifestations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol	Name
ATRNL1	attractin-like 1
C20ORF196	chromosome 20 open reading frame 196
CRTC3	CREB regulated transcription coactivator 3
DCDC2	doublecortin domain containing 2
FAM110C	family with sequence similarity 110, member C
KCTD2	potassium channel tetramerization domain containing 2
MYRIP	myosin VIIA and Rab interacting protein
PKNOX1	PBX/knotted 1 homeobox 1
TMEM245	transmembrane protein 245