ELOC, elongin C, 6921

N. diseases: 41; N. variants: 3
Disease: Nonnuclear polymorphic congenital cataract ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3888391
Disease: Nonnuclear polymorphic congenital cataract
Nonnuclear polymorphic congenital cataract 		0.010 GeneticVariation disease BEFREE PCC is triggered by mutations which disrupt interactions at the elongin C binding site. 19408298 2009