CFH, complement factor H, 3075

N. diseases: 393; N. variants: 150
Disease: Retinal thrombosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1579873
Disease: Retinal thrombosis
Retinal thrombosis 		0.010 GeneticVariation disease BEFREE Complement Factor H Mutation W1206R Causes Retinal Thrombosis and Ischemic Retinopathy in Mice. 30711487 2019