Disease: Aura ×
Source: ALL
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 GRIN2A mutations cause epilepsy-aphasia spectrum disorders. 23933818 2013
CUI: C0236018
Disease: Aura
Aura 		0.300 Biomarker phenotype CTD_human Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. 20890276 2010