renpenning syndrome Gene Set

Dataset	DISEASES Text-mining Gene-Disease Association Evidence Scores
Category	disease or phenotype associations
Type	disease
Description	An intellectual disability that is characterized by small head size (microcephaly), long narrow face, short stature, small testes, and intellectual deficit which follows X-linked inheritance and presents most often in males. (Human Disease Ontology, DOID_0060179)
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Genes

11 genes co-occuring with the disease renpenning syndrome 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