Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4520981
Disease: Abnormality of the basal ganglia
Abnormality of the basal ganglia
0.100 GeneticVariation phenotype CLINVAR Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype-phenotype correlation. 24785942 2014