GAL, galanin and GMAP prepropeptide, 51083

N. diseases: 226; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0016952
Disease: Galactosemias
Galactosemias
0.050 Biomarker disease BEFREE Results revealed that Gal-1-P is not the sole pathophysiological agent responsible for the phenotype observed in galactosemia. 31808946 2019
CUI: C0016952
Disease: Galactosemias
Galactosemias
0.050 Biomarker disease BEFREE Galactokinase (GALK1) is the enzyme responsible for converting galactose into gal-1-p. A pharmacological inhibitor of GALK1 is hypothesized to be therapeutic strategy for treating galactosemia by reducing production of gal-1-p. 30806949 2019
CUI: C0016952
Disease: Galactosemias
Galactosemias
0.050 AlteredExpression disease BEFREE RBC gal-1-p and urine galactitol were monitored during the follow-up visits in every child with DG galactosemia. 18976948 2008
CUI: C0016952
Disease: Galactosemias
Galactosemias
0.050 Biomarker disease BEFREE The value of measuring Gal-1-P concentrations routinely once successfully established on a galactosaemia diet is questionable as concentrations do not appear to affect outcome. 10952646 2000
CUI: C0016952
Disease: Galactosemias
Galactosemias
0.050 GeneticVariation disease BEFREE The development of POF in females with galactosemia is more likely if the patient's genotype is Q188R/Q188R, if the mean erythrocyte Gal-1-P is >3.5 mg/dL during therapy, and if the recovery of (13)CO(2) from whole-body (13)C-galactose oxidation is reduced below 5% of administered (13)C-galactose. 11113841 2000