OTX1, orthodenticle homeobox 1, 5013

N. diseases: 35; N. variants: 1
Disease: Reading Disabilities ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0871215
Disease: Reading Disabilities
Reading Disabilities 		0.010 GeneticVariation disease BEFREE Our data therefore suggest that linkage with reading disability at 2p12-16 is not caused by coding variants of SEMA4F or OTX1. 11901358 2002