Disease: Idiopathic non-cirrhotic portal hypertension ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4476912
Disease: Idiopathic non-cirrhotic portal hypertension
Idiopathic non-cirrhotic portal hypertension 		0.010 GeneticVariation disease BEFREE The autosomal dominant inheritance in this unique pedigree and the single de novo mutation identified, strongly suggests that KCNN3 mutations have a pathogenetic role in INCPH. 26658685 2016