LGALS14, galectin 14, 56891

N. diseases: 35; N. variants: 1
Disease: Epilepsy, Generalized ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized 		0.010 GeneticVariation disease BEFREE Functional evaluation of human ClC-2 chloride channel mutations associated with idiopathic generalized epilepsies. 15252188 2004