Disease: Hereditary X-Linked Recessive Spastic Paraplegia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0751604
Disease: Hereditary X-Linked Recessive Spastic Paraplegia
Hereditary X-Linked Recessive Spastic Paraplegia 		0.300 Biomarker disease CTD_human Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesis. 23176824 2012