Neonatal Abstinence Syndrome Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A withdrawal disorder that is characterized by a group of problems that occur in a newborn who was exposed to addictive illegal or prescription drugs while in the mother's womb or postnatally following the discontinuance of drug treatment. (Human Disease Ontology, DOID_9828)
External Link	https://www.disgenet.org/browser/0/1/0/C0027609
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Genes

9 genes associated with the disease Neonatal Abstinence Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
ABCB1	ATP-binding cassette, sub-family B (MDR/TAP), member 1
BDNF	brain-derived neurotrophic factor
COMT	catechol-O-methyltransferase
CYP2B6	cytochrome P450, family 2, subfamily B, polypeptide 6
INSRR	insulin receptor-related receptor
NUCB2	nucleobindin 2
OPRK1	opioid receptor, kappa 1
OPRM1	opioid receptor, mu 1
PNOC	prepronociceptin