Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8818
Gene Symbol: DPM2
DPM2
CUI: C3554385
Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu 		0.700 Biomarker GENOMICS_ENGLAND Electroclinical Features of Early-Onset Epileptic Encephalopathies in Congenital Disorders of Glycosylation (CDGs). 26453362

2016
Entrez Id: 8818
Gene Symbol: DPM2
DPM2
CUI: C3554385
Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu 		0.700 Biomarker GENOMICS_ENGLAND DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy. 23109149

2012
Entrez Id: 8818
Gene Symbol: DPM2
DPM2
CUI: C3554385
Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu 		0.700 Biomarker GENOMICS_ENGLAND DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy. 23109149

2012
Entrez Id: 8818
Gene Symbol: DPM2
DPM2
CUI: C3554385
Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu 		0.700 Biomarker GENOMICS_ENGLAND DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy. 23109149

2012
Entrez Id: 8818
Gene Symbol: DPM2
DPM2
CUI: C3554385
Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu 		0.700 Biomarker GENOMICS_ENGLAND Congenital muscular dystrophy with defective alpha-dystroglycan, cerebellar hypoplasia, and epilepsy. 19901254

2009
Entrez Id: 8818
Gene Symbol: DPM2
DPM2
CUI: C0036572
Disease: Seizures
Seizures 		0.400 Biomarker GENOMICS_ENGLAND Electroclinical Features of Early-Onset Epileptic Encephalopathies in Congenital Disorders of Glycosylation (CDGs). 26453362

2016