Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1856019
Disease: Abnormal cortical gyration
Abnormal cortical gyration
0.100 CausalMutation phenotype CLINVAR Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism. 27159400 2016