SLC25A13, solute carrier family 25 member 13, 10165

N. diseases: 109; N. variants: 23
Disease: Steatohepatitis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis 		0.130 GeneticVariation disease BEFREE The prevalence of hepatic steatosis in 19 CTLN2 patients was examined, and clinical features were compared with those of non-alcoholic fatty liver disease (NAFLD) patients without known SLC25A13 gene mutations. 18620775 2008
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis 		0.130 GeneticVariation disease BEFREE Six patients with hepatic steatosis participated in the genetic study for the SLC25A13 gene under parental consent. 16737877 2006
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis 		0.130 GeneticVariation disease BEFREE Homozygous SLC25A13 mutation in a Taiwanese patient with adult-onset citrullinemia complicated with steatosis and hepatocellular carcinoma. 17000460 2006
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis 		0.130 Biomarker disease HPO