DCX, doublecortin, 1641

N. diseases: 175; N. variants: 107
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0238111
Disease: Lennox-Gastaut syndrome
Lennox-Gastaut syndrome
0.010 GeneticVariation disease BEFREE Familial Lennox-Gastaut syndrome in male siblings with a novel DCX mutation and anterior pachygyria. 20726879 2010