Disease Term Disease ID Gene Symbol Classification References Source
Autosomal dominant primary hypomagnesemia with hypocalciuria 34528 FXYD2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
HNF1B Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -