Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0008370
Disease: Cholestasis
Cholestasis
0.080 Biomarker disease BEFREE MYO5B deficiency may underlie 20% of previously undiagnosed low-GGT cholestasis. 28027573 2017
CUI: C0008370
Disease: Cholestasis
Cholestasis
0.080 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
0.080 Biomarker disease BEFREE Genetic defects in ATP8B1 or ABCB11 account for the majority of cholestasis with low GGT. 27050426 2016
CUI: C0008370
Disease: Cholestasis
Cholestasis
0.080 Biomarker disease BEFREE This study aimed to evaluate the role of GGT as a screening marker among diverse etiologies of infantile cholestasis. 25141230 2014
CUI: C0008370
Disease: Cholestasis
Cholestasis
0.080 Biomarker 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
0.080 Biomarker disease BEFREE Cholestasis with normal GGT developed 17 and 4.8years after liver transplantation, in patient 1 and patient 2, respectively, during an immunosuppression reduction period. 20800306 2010
CUI: C0008370
Disease: Cholestasis
Cholestasis
0.080 Biomarker disease BEFREE An appropriate medical evaluation and particular consideration of AGS is essential before surgical referral in infants with high GGT cholestasis. 20601899 2010
CUI: C0008370
Disease: Cholestasis
Cholestasis
0.080 Biomarker disease BEFREE Benign recurrent intrahepatic cholestasis progressing to progressive familial intrahepatic cholestasis: low GGT cholestasis is a clinical continuum. 11867191 2002