TBP, TATA-box binding protein, 6908

N. diseases: 158; N. variants: 3
Disease: Cerebral cortical atrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy 		0.010 Biomarker disease BEFREE The SCA17 clinical phenotype includes characteristics associated with cerebellar and cortical atrophy such as ataxia, dementia, epilepsy, chorea and parkinsonian features. 21710129 2011