alcohol-related neurodevelopmental disorder Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A fetal alcohol spectrum disorder that results in central nervous system dysfunction and behavioral and/or cognitive deficits due to prenatal alcohol exposure. (Human Disease Ontology, DOID_0050667)
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26 genes co-occuring with the disease alcohol-related neurodevelopmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PFAS phosphoribosylformylglycinamidine synthase 2.59846
WDR45 WD repeat domain 45 2.3644
BOLA3 bolA family member 3 1.53392
WIPI1 WD repeat domain, phosphoinositide interacting 1 1.37425
GRID2 glutamate receptor, ionotropic, delta 2 1.33807
LIAS lipoic acid synthetase 1.28479
GLRX5 glutaredoxin 5 1.27693
RNASET2 ribonuclease T2 1.23256
GCSH glycine cleavage system protein H (aminomethyl carrier) 1.22172
FA2H fatty acid 2-hydroxylase 1.14517
GLDC glycine dehydrogenase (decarboxylating) 1.06732
SNAP25 synaptosomal-associated protein, 25kDa 1.04377
BOC BOC cell adhesion associated, oncogene regulated 0.879014
B4GALNT2 beta-1,4-N-acetyl-galactosaminyl transferase 2 0.8741
NSF N-ethylmaleimide-sensitive factor 0.801154
ATRX alpha thalassemia/mental retardation syndrome X-linked 0.644192
GRIN2A glutamate receptor, ionotropic, N-methyl D-aspartate 2A 0.617486
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B 0.500379
MYOG myogenin (myogenic factor 4) 0.481325
PER2 period circadian clock 2 0.440914
HEXA hexosaminidase A (alpha polypeptide) 0.427015
PER1 period circadian clock 1 0.413527
MGP matrix Gla protein 0.369628
NES nestin 0.332487
ASRGL1 asparaginase like 1 0.313552
PLA2G1B phospholipase A2, group IB (pancreas) 0.278297