DLX1, distal-less homeobox 1, 1745

N. diseases: 30; N. variants: 0
Disease: Autism Spectrum Disorders ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		0.310 GeneticVariation disease BEFREE A rare haplotype in the DLX1 promoter was associated with ASD (P-value = 0.001). 21302352 2011
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		0.310 Biomarker disease CTD_human A rare haplotype in the DLX1 promoter was associated with ASD (P-value = 0.001). 21302352 2011