SPRTN, SprT-like N-terminal domain, 83932

N. diseases: 44; N. variants: 3
Disease: Progeria ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0033300
Disease: Progeria
Progeria 		0.300 Biomarker disease CTD_human Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid features. 25261934 2014