Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 170302
Gene Symbol: ARX
ARX
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.020 GeneticVariation BEFREE ARX mutation testing should be undertaken in children aged less than 1 year with Ohtahara syndrome and a movement disorder, and in infants with unexplained neurodegeneration, progressive white matter loss, and cortical atrophy. 19747203

2010
Entrez Id: 170302
Gene Symbol: ARX
ARX
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.020 Biomarker LHGDN This combination of early infantile spasms followed by a complex movement disorder contributes further to extent the pleiotropy of the ARX-linked "interneuronopathy" and should lead the clinician to ARX mutation screening. 18468866

2008
Entrez Id: 170302
Gene Symbol: ARX
ARX
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.020 Biomarker BEFREE This combination of early infantile spasms followed by a complex movement disorder contributes further to extent the pleiotropy of the ARX-linked "interneuronopathy" and should lead the clinician to ARX mutation screening. 18468866

2008