OTX1, orthodenticle homeobox 1, 5013

N. diseases: 35; N. variants: 1
Disease: Dyslexia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0476254
Disease: Dyslexia
Dyslexia 		0.010 GeneticVariation disease BEFREE Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1. 11901358 2002