Disease: Hypocalciuria ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020599
Disease: Hypocalciuria
Hypocalciuria 		0.010 GeneticVariation phenotype BEFREE We suggest that the upregulation of TRPV5/6 and of ROMK1 and Maxi-K may contribute to hypocalciuria and hypokalemia in Ncc Ser707X knockin mice and human GS, respectively. 20848653 2010