Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 79947
Gene Symbol: DHDDS
DHDDS 		0.600 GeneticVariation disease UNIPROT High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies. 29100083 2017
Entrez Id: 79947
Gene Symbol: DHDDS
DHDDS 		0.600 Biomarker disease GENOMICS_ENGLAND High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies. 29100083 2017
Entrez Id: 79947
Gene Symbol: DHDDS
DHDDS 		0.600 Biomarker disease GENOMICS_ENGLAND A case of fatal Type I congenital disorders of glycosylation (CDG I) associated with low dehydrodolichol diphosphate synthase (DHDDS) activity. 27343064 2016
Entrez Id: 79947
Gene Symbol: DHDDS
DHDDS 		0.600 CausalMutation disease CLINVAR