ARX, aristaless related homeobox, 170302

N. diseases: 249; N. variants: 44
Disease: FOXG1 syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		0.010 Biomarker disease BEFREE FOXG1 syndrome is as an epileptic-dyskinetic encephalopathy whose clinical presentation bears similarities with ARX- and STXBP1-gene related encephalopathies. 26344814 2016