DPP6, dipeptidyl peptidase like 6, 1804

N. diseases: 71; N. variants: 24
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0431350
Disease: Primary microcephaly
Primary microcephaly
0.300 Biomarker disease GENOMICS_ENGLAND Loss-of-function variation in the DPP6 gene is associated with autosomal dominant microcephaly and mental retardation. 23832105 2013