CHGB, chromogranin B, 1114

N. diseases: 70; N. variants: 3
Disease: Amyotrophic Lateral Sclerosis, Sporadic ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1862941
Disease: Amyotrophic Lateral Sclerosis, Sporadic
Amyotrophic Lateral Sclerosis, Sporadic 		0.010 GeneticVariation disease BEFREE The P413L chromogranin B variation in French patients with sporadic amyotrophic lateral sclerosis. 20932227 2011