Disease: Paraplegia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0030486
Disease: Paraplegia
Paraplegia 		0.010 GeneticVariation disease LHGDN Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia. 14564668 2003