WNT2B, Wnt family member 2B, 7482

N. diseases: 65; N. variants: 12
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011991
Disease: Diarrhea
Diarrhea
0.110 CausalMutation phenotype CLINVAR
CUI: C0011991
Disease: Diarrhea
Diarrhea
0.110 Biomarker phenotype HPO
CUI: C0011991
Disease: Diarrhea
Diarrhea
0.110 Biomarker phenotype BEFREE WNT2B deficiency should be considered for individuals with neonatal-onset diarrhea. 29909964 2018