HNF1B, HNF1 homeobox B, 6928

N. diseases: 22; N. variants: 67
Source: CURATED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1835171
Disease: Hypomagnesemia 2, renal
Hypomagnesemia 2, renal
0.330 GermlineCausalMutation disease ORPHANET HNF1B mutations associate with hypomagnesemia and renal magnesium wasting. 19389850 2009