Disease: Paraparesis, Spastic ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0037771
Disease: Paraparesis, Spastic
Paraparesis, Spastic 		0.120 GeneticVariation phenotype BEFREE Paraplegin mutations are a frequent cause of sporadic spastic paraparesis. 18799786 2008
CUI: C0037771
Disease: Paraparesis, Spastic
Paraparesis, Spastic 		0.120 GeneticVariation phenotype LHGDN Paraplegin mutations are a frequent cause of sporadic spastic paraparesis. 18799786 2008
CUI: C0037771
Disease: Paraparesis, Spastic
Paraparesis, Spastic 		0.120 GeneticVariation phenotype LHGDN The new SPG7 gene mutation leads to a novel complicated autosomal recessive hereditary spastic paraparesis phenotype that widens the spectrum of different brain systems that are optionally affected in hereditary spastic paraplegia (HSP). 17646629 2007
CUI: C0037771
Disease: Paraparesis, Spastic
Paraparesis, Spastic 		0.120 CausalMutation phenotype CLINVAR