Disease: Cholestasis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0008370
Disease: Cholestasis
Cholestasis 		0.100 Biomarker disease BEFREE All presented with high gamma-glutamyl transpeptidase cholestasis and hepatitis. 30628989 2019
CUI: C0008370
Disease: Cholestasis
Cholestasis 		0.100 Biomarker disease BEFREE The results revealed that the serum levels of alanine aminotransferase, aspartate aminotransferase, total bilirubin, direct bilirubin, γ‑glutamyl transpeptidase, and alkaline phosphatase were reduced in rats with ANIT‑induced cholestasis that were treated with MT. 30226547 2018
CUI: C0008370
Disease: Cholestasis
Cholestasis 		0.100 Biomarker disease BEFREE Marker for cholestasis as total and individual serum BAs, bilirubin, alkaline phosphatase (AP), and gamma-glutamyl transpeptidase (GGT) were analyzed in patients screened for HPS. 27951601 2017
CUI: C0008370
Disease: Cholestasis
Cholestasis 		0.100 AlteredExpression disease BEFREE Cholestasis occurred before (n = 5) or after (n = 3) ITx and was characterized by intermittent jaundice, intractable pruritus, increased serum bile acid (BA) levels, and normal gamma-glutamyl transpeptidase activity. 24375397 2014
CUI: C0008370
Disease: Cholestasis
Cholestasis 		0.100 GeneticVariation disease BEFREE As low or normal gamma-glutamyl transpeptidase (GGT) activity has been described in all patients with ARC syndrome identified so far, ARC syndrome is a possible diagnosis for low GGT cholestasis. 24782640 2014
CUI: C0008370
Disease: Cholestasis
Cholestasis 		0.100 Biomarker disease BEFREE Alagille syndrome (AGS) frequently presents with neonatal jaundice and can mimic other causes of high gamma-glutamyl transpeptidase (GGT) cholestasis, most notably biliary atresia. 20601899 2010
CUI: C0008370
Disease: Cholestasis
Cholestasis 		0.100 Biomarker disease BEFREE We describe the clinical course of 6 patients who developed recurrent low gamma-glutamyl transpeptidase cholestasis, that mimicks BSEP disease, following transplantation. 20583290 2010
CUI: C0008370
Disease: Cholestasis
Cholestasis 		0.100 Biomarker disease BEFREE Homozygous mutations in the ATP8B1 gene cause cholestasis with a normal serum gamma-glutamyl transpeptidase (gamma-GT), and have been reported in two forms of cholestasis: progressive familial intrahepatic cholestasis type 1 (PFIC1) and benign recurrent intrahepatic cholestasis (BRIC). 15888793 2005
CUI: C0008370
Disease: Cholestasis
Cholestasis 		0.100 Biomarker disease BEFREE The present case, which accumulates the 3 clinical disorders assocaited with MDR3 deficiency, shows that this condition should be suspected not only in children or young people with high gamma-glutamyl transpeptidase cholestasis but also in middle-aged or older patients with chronic idiopathic cholestasis, especially when there is a previous history of cholestasis of pregnancy or juvenile cholelithiasis. 12671900 2003
CUI: C0008370
Disease: Cholestasis
Cholestasis 		0.100 Biomarker disease BEFREE Biochemical liver abnormalities are consistent with the presence of cholestasis and include an elevation of both serum alkaline phosphatase and gamma-glutamyl transpeptidase, with or without elevation of aminotransferase levels. 11918275 2001