APP, amyloid beta precursor protein, 351

N. diseases: 384; N. variants: 105
Disease: Ataxia, Spinocerebellar ×
Source: BEFREE ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0087012
Disease: Ataxia, Spinocerebellar
Ataxia, Spinocerebellar 		0.010 Biomarker disease BEFREE Mutations in genes encoding subunits of the m-AAA protease have been linked to various neurodegenerative diseases in humans, such as hereditary spastic paraplegia and spinocerebellar ataxia. 27911893 2016