Source: CTD_human

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6573
Gene Symbol: SLC19A1
SLC19A1
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.310 Biomarker CTD_human A functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autism. 20468076

2010
Entrez Id: 6573
Gene Symbol: SLC19A1
SLC19A1
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.310 Biomarker CTD_human Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism. 16917939

2006