GCK, glucokinase, 2645

N. diseases: 210; N. variants: 182
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.120 GeneticVariation phenotype BEFREE Strict maternal euglycaemia can contribute to intrauterine growth restriction and low BW when the foetus has inherited the GCK mutation from the mother. 18248649 2008
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.120 Biomarker phenotype BEFREE The five subjects with permanent neonatal diabetes due to glucokinase deficiency identified to date are characterized by intrauterine growth retardation, permanent insulin-requiring diabetes from the first day of life, and hyperglycemia in both parents. 14578306 2003
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
0.120 Biomarker phenotype HPO