CTNND2, catenin delta 2, 1501

N. diseases: 117; N. variants: 18
Disease: EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1 ×
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C1832841
Disease: EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1 		disease Nervous System Diseases Disease or Syndrome 4 0.300 None 1.000 1 2017 2017