Disease: Paraplegia, Spinal ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0278115
Disease: Paraplegia, Spinal
Paraplegia, Spinal 		0.300 Biomarker phenotype CTD_human Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein. 11549317 2001