Disease: Brain atrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4551584
Disease: Brain atrophy
Brain atrophy 		0.110 GeneticVariation disease BEFREE Homozygous GRID2 missense mutation predicts a shift in the D-serine binding domain of GluD2 in a case with generalized brain atrophy and unusual clinical features. 29207948 2017
CUI: C4551584
Disease: Brain atrophy
Brain atrophy 		0.110 Biomarker disease HPO