PVALB, parvalbumin, 5816

N. diseases: 148; N. variants: 0
Disease: Gitelman Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0268450
Disease: Gitelman Syndrome
Gitelman Syndrome 		0.010 GeneticVariation disease LHGDN The renal phenotype of the parvalbumin knockout mice pointed to PVALB as a candidate gene for GS for SLC12A3-negative cases. 18469313 2008
CUI: C0268450
Disease: Gitelman Syndrome
Gitelman Syndrome 		0.010 Biomarker disease BEFREE The renal phenotype of the parvalbumin knockout mice pointed to PVALB as a candidate gene for GS for SLC12A3-negative cases. 18469313 2008