SERPINI1, serpin family I member 1, 5274

N. diseases: 58; N. variants: 7
Disease: Familial Dementia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0751071
Disease: Familial Dementia
Familial Dementia 		0.020 GeneticVariation disease BEFREE Point mutations in the neuroserpin gene cause the autosomal dominant dementia familial encephalopathy with neuroserpin inclusion bodies or FENIB. 21115126 2011
CUI: C0751071
Disease: Familial Dementia
Familial Dementia 		0.020 GeneticVariation disease BEFREE The dementia familial encephalopathy with neuroserpin inclusion bodies (FENIB) is caused by point mutations in the neuroserpin gene. 15291813 2004