NEUROG3, neurogenin 3, 50674

N. diseases: 49; N. variants: 8
Disease: Diarrhea 4, Malabsorptive, Congenital ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1835888
Disease: Diarrhea 4, Malabsorptive, Congenital
Diarrhea 4, Malabsorptive, Congenital 		0.700 GermlineCausalMutation disease ORPHANET Mutant neurogenin-3 in congenital malabsorptive diarrhea. 16855267 2006
CUI: C1835888
Disease: Diarrhea 4, Malabsorptive, Congenital
Diarrhea 4, Malabsorptive, Congenital 		0.700 GeneticVariation disease UNIPROT Mutant neurogenin-3 in congenital malabsorptive diarrhea. 16855267 2006
CUI: C1835888
Disease: Diarrhea 4, Malabsorptive, Congenital
Diarrhea 4, Malabsorptive, Congenital 		0.700 Biomarker disease CTD_human
CUI: C1835888
Disease: Diarrhea 4, Malabsorptive, Congenital
Diarrhea 4, Malabsorptive, Congenital 		0.700 CausalMutation disease CLINVAR