Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4691
Gene Symbol: NCL
NCL
0.020 Biomarker disease BEFREE Two types of NCL have so-far been found almost exclusively in Finland: Finnish variant late infantile NCL, vLINCL (CLN5), and the Northern epilepsy syndrome or Progressive epilepsy with mental retardation, EPMR (CLN8). 11332769 2001
Entrez Id: 4691
Gene Symbol: NCL
NCL
0.020 Biomarker disease BEFREE A missense mutation in CLN8 causes progressive epilepsy with mental retardation (EPMR) or Northern epilepsy, which has so far been reported only from Finland and is now classified as an NCL. 11589000 2001