Disease: Pervasive Development Disorder ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.060 Biomarker group BEFREE MET mediates its specific biological effects through different intracellular signaling pathways and has a complex protein interactome that is enriched in autism spectrum disorder and other NDD candidates. 27837921 2017
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.060 GeneticVariation group BEFREE Autism spectrum disorder: interaction of air pollution with the MET receptor tyrosine kinase gene. 24240654 2014
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.060 GeneticVariation group BEFREE A familial heterozygous null mutation of MET in autism spectrum disorder. 24909855 2014
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.060 Biomarker group BEFREE Association of MET with social and communication phenotypes in individuals with autism spectrum disorder. 19548256 2010
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.060 GeneticVariation group BEFREE Stratification by the presence of gastrointestinal conditions revealed that the MET C allele was associated with both autism spectrum disorder and gastrointestinal conditions in 118 families containing at least 1 child with co-occurring autism spectrum disorder and gastrointestinal conditions. 19255034 2009
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.060 GeneticVariation group BEFREE Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder. 19360663 2008