DCX, doublecortin, 1641

N. diseases: 175; N. variants: 107
Disease: Abnormal cortical gyration ×
Source: ALL
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
CUI: C1856019
Disease: Abnormal cortical gyration
Abnormal cortical gyration 		0.100 GeneticVariation phenotype CLINVAR