CNTN2, contactin 2, 6900

N. diseases: 99; N. variants: 14
Disease: Tremor ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0040822
Disease: Tremor
Tremor 		0.110 GeneticVariation phenotype BEFREE Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2. 23518707 2013
CUI: C0040822
Disease: Tremor
Tremor 		0.110 Biomarker phenotype HPO