Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.030 GeneticVariation disease BEFREE The gene for solute carrier family 18 member A1 (vesicular monoamine transporter; SLC18A1) is of particular interest in this regard because of its association with schizophrenia, autism and bipolar illness as well as with cancer. 30194079 2018
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.030 GeneticVariation disease BEFREE Association study of the vesicular monoamine transporter 1 (VMAT1) gene with autism in an Iranian population. 28476685 2017
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.030 Biomarker disease BEFREE The JARID1C-regulated genes SCN2A, CACNA1H, BDNF, and SLC18A1 have previously been associated with autism and cognitive dysfunction. 18203167 2008