Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0236018
Disease: Aura
Aura
0.300 Biomarker phenotype CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082 2018
CUI: C0236018
Disease: Aura
Aura
0.300 Biomarker phenotype CTD_human GABAA receptor beta3 subunit gene-deficient heterozygous mice show parent-of-origin and gender-related differences in beta3 subunit levels, EEG, and behavior. 15878204 2005