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 		0.310 Biomarker phenotype CTD_human The discovered TECPR2 mutation implicates autophagy, a central intracellular mechanism, in spastic paraparesis. 23176824 2012
CUI: C0037771
Disease: Paraparesis, Spastic
Paraparesis, Spastic 		0.310 GeneticVariation phenotype BEFREE The discovered TECPR2 mutation implicates autophagy, a central intracellular mechanism, in spastic paraparesis. 23176824 2012