HNF1B, HNF1 homeobox B, 6928

N. diseases: 279; N. variants: 72
Disease: bilateral agenesis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0332910
Disease: bilateral agenesis
bilateral agenesis 		0.010 GeneticVariation disease BEFREE Various renal phenotypes were observed, but no case of bilateral agenesis was associated with HNF1B or PAX2 mutations. 23539225 2013