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 		0.030 GeneticVariation group BEFREE Mutations in interleukin-1 receptor accessory protein like 1 (IL1RAPL1) gene have been associated with non-syndromic intellectual disability (ID) and autism spectrum disorder. 25305082 2015
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.030 GeneticVariation group BEFREE Intragenic deletions of IL1RAPL1, only rarely identified, have mostly been associated with nonspecific intellectual disability (IDX) and autism spectrum disorder. 23613341 2013
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.030 Biomarker group BEFREE Interleukin-1 receptor accessory protein-like 1 (IL1RAPL1) is associated with X-linked mental retardation and autism spectrum disorder. 23785489 2013