Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 50674
Gene Symbol: NEUROG3
NEUROG3
0.140 GeneticVariation phenotype BEFREE Four patients (two males, two females) were diagnosed with homozygous mutations in NEUROG3 on the basis of congenital malabsorptive diarrhea and diabetes. 27533310 2016
Entrez Id: 50674
Gene Symbol: NEUROG3
NEUROG3
0.140 GeneticVariation phenotype BEFREE We hypothesized that null mutations in NEUROG3 might be responsible for the disease in a patient with permanent neonatal diabetes and severe congenital malabsorptive diarrhea. 21378176 2011
Entrez Id: 50674
Gene Symbol: NEUROG3
NEUROG3
0.140 GeneticVariation phenotype BEFREE This report describes a newly identified nonsense mutation in human NEUROG3 that in the homozygous state is associated with neonatal diabetes and malabsorptive diarrhea. 21490072 2011
Entrez Id: 50674
Gene Symbol: NEUROG3
NEUROG3
0.140 GeneticVariation phenotype BEFREE A newly discovered disorder characterized by malabsorptive diarrhea and a lack of intestinal enteroendocrine cells is caused by loss-of-function mutations in NEUROG3. 16855267 2006
Entrez Id: 50674
Gene Symbol: NEUROG3
NEUROG3
0.140 Biomarker phenotype HPO