Disease: Leber plus disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4304725
Disease: Leber plus disease
Leber plus disease 		0.300 GermlineCausalMutation disease ORPHANET Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia. 8644732 1996