CTNND2, catenin delta 2, 1501

N. diseases: 117; N. variants: 18
Disease: Familial (FPAH) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 GeneticVariation disease BEFREE δ-Catenin (<i>CTNND2</i>) missense mutation in familial cortical myoclonic tremor and epilepsy. 29127138 2017