Gene: CNTF ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1270
Gene Symbol: CNTF
CNTF 		0.310 Biomarker disease CTD_human Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene. 11951178 2002
Entrez Id: 1270
Gene Symbol: CNTF
CNTF 		0.310 GeneticVariation disease BEFREE In addition, patients with sporadic amyotrophic lateral sclerosis who had a homozygous CNTF gene defect showed significantly earlier disease onset but did not show a significant difference in disease duration. 11951178 2002