ACOT13, acyl-CoA thioesterase 13, 55856

N. diseases: 17; N. variants: 0
Disease: Dyslexia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0476254
Disease: Dyslexia
Dyslexia 		0.020 GeneticVariation disease BEFREE Interestingly, healthy subjects bearing the KIAA0319/TTRAP/THEM2 variants previously identified as enhancing the risk of dyslexia showed a reduced left-hemispheric asymmetry of the STS. 22262880 2012
CUI: C0476254
Disease: Dyslexia
Dyslexia 		0.020 GeneticVariation disease BEFREE We have recently identified a risk haplotype associated with dyslexia on chromosome 6p22.2 which spans the TTRAP gene and portions of THEM2 and KIAA0319. 16600991 2006