syndromic intellectual disability Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An intellectual disability that is characterized by the presence of associated medical and behavioral sign and symptoms. (Human Disease Ontology, DOID_0050888)
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11 genes co-occuring with the disease syndromic intellectual disability in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PQBP1 polyglutamine binding protein 1 2.7544
WBP11 WW domain binding protein 11 2.43927
CDX4 caudal type homeobox 4 1.58359
OPHN1 oligophrenin 1 1.21348
DLG3 discs, large homolog 3 (Drosophila) 1.15965
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter) 1.0627
MLXIPL MLX interacting protein-like 0.921323
FGF4 fibroblast growth factor 4 0.825358
ATRX alpha thalassemia/mental retardation syndrome X-linked 0.822897
MECP2 methyl CpG binding protein 2 0.540055
FGFR2 fibroblast growth factor receptor 2 0.476014