DCX, doublecortin, 1641

N. diseases: 175; N. variants: 107
Disease: Epilepsy, Cryptogenic ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0086237
Disease: Epilepsy, Cryptogenic
Epilepsy, Cryptogenic 		0.010 GeneticVariation disease BEFREE Nonsyndromic mental retardation and cryptogenic epilepsy in women with doublecortin gene mutations. 12838518 2003