DPP6, dipeptidyl peptidase like 6, 1804

N. diseases: 71; N. variants: 24
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 33 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4225375
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 33
MENTAL RETARDATION, AUTOSOMAL DOMINANT 33 		0.700 GeneticVariation disease UNIPROT Loss-of-function variation in the DPP6 gene is associated with autosomal dominant microcephaly and mental retardation. 23832105 2013
CUI: C4225375
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 33
MENTAL RETARDATION, AUTOSOMAL DOMINANT 33 		0.700 Biomarker disease GENOMICS_ENGLAND Loss-of-function variation in the DPP6 gene is associated with autosomal dominant microcephaly and mental retardation. 23832105 2013
CUI: C4225375
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 33
MENTAL RETARDATION, AUTOSOMAL DOMINANT 33 		0.700 Biomarker disease CTD_human
CUI: C4225375
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 33
MENTAL RETARDATION, AUTOSOMAL DOMINANT 33 		0.700 CausalMutation disease CLINVAR