Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4310738
Disease: MEIER-GORLIN SYNDROME 7
MEIER-GORLIN SYNDROME 7
0.600 GeneticVariation disease UNIPROT Mutations in CDC45, Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and Craniosynostosis. 27374770 2016
CUI: C4310738
Disease: MEIER-GORLIN SYNDROME 7
MEIER-GORLIN SYNDROME 7
0.600 Biomarker disease GENOMICS_ENGLAND Mutations in CDC45, Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and Craniosynostosis. 27374770 2016
CUI: C4310738
Disease: MEIER-GORLIN SYNDROME 7
MEIER-GORLIN SYNDROME 7
0.600 GeneticVariation disease CLINVAR Mutations in CDC45, Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and Craniosynostosis. 27374770 2016
CUI: C4310738
Disease: MEIER-GORLIN SYNDROME 7
MEIER-GORLIN SYNDROME 7
0.600 Biomarker disease GENOMICS_ENGLAND Factors influencing success of clinical genome sequencing across a broad spectrum of disorders. 25985138 2015
CUI: C4310738
Disease: MEIER-GORLIN SYNDROME 7
MEIER-GORLIN SYNDROME 7
0.600 CausalMutation disease CLINVAR