Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		0.200 Biomarker disease MGD A quantitative survey of gravity receptor function in mutant mouse strains. 16235133 2005
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		0.200 Biomarker disease MGD Postural and locomotor control in normal and vestibularly deficient mice. 15243133 2004
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		0.200 Biomarker disease MGD Altered potassium balance and aldosterone secretion in a mouse model of human congenital long QT syndrome. 11438691 2001
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		0.200 Biomarker disease MGD KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells. 11223304 2001
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		0.200 Biomarker disease MGD A new spontaneous mouse mutation in the Kcne1 gene. 11003695 2000
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		0.200 Biomarker disease MGD Inner ear defects induced by null mutation of the isk gene. 8982171 1996