CDH15, cadherin 15, 1013

N. diseases: 38; N. variants: 5
Disease: Mental Retardation, Autosomal Dominant 3 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2675488
Disease: Mental Retardation, Autosomal Dominant 3
Mental Retardation, Autosomal Dominant 3 		0.600 Biomarker disease GENOMICS_ENGLAND Penetrance of pathogenic mutations in haploinsufficient genes for intellectual disability and related disorders. 26506440 2015
CUI: C2675488
Disease: Mental Retardation, Autosomal Dominant 3
Mental Retardation, Autosomal Dominant 3 		0.600 GeneticVariation disease UNIPROT Alterations in CDH15 and KIRREL3 in patients with mild to severe intellectual disability. 19012874 2008
CUI: C2675488
Disease: Mental Retardation, Autosomal Dominant 3
Mental Retardation, Autosomal Dominant 3 		0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C2675488
Disease: Mental Retardation, Autosomal Dominant 3
Mental Retardation, Autosomal Dominant 3 		0.600 Biomarker disease CTD_human