HNF1B, HNF1 homeobox B, 6928

N. diseases: 279; N. variants: 72
Disease: Polyuria ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0032617
Disease: Polyuria
Polyuria 		0.010 GeneticVariation phenotype BEFREE In the absence of maternal diabetes, HNF1B mutation can be associated with polyhydramnios, probably due to fetal polyuria. 27286685 2016