Gene: SPG11 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.040 GeneticVariation disease BEFREE A pair of monozygotic 22-year-old twins with complicated hereditary spastic paraplegia caused by a novel SPG11 mutation is described. 28991695 2017
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.040 Biomarker disease BEFREE Although SPG11 is the most common complicated hereditary spastic paraplegia, our knowledge of the long-term prognosis and life expectancy is limited. 23443022 2013
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.040 Biomarker disease BEFREE Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia. 19917823 2009
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.040 GeneticVariation disease BEFREE SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegia. 18337587 2008