Gene: CFH ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3075
Gene Symbol: CFH
CFH 		0.020 GeneticVariation group BEFREE Complement factor H 402H variant and reticular macular disease. 21825189 2011
Entrez Id: 3075
Gene Symbol: CFH
CFH 		0.020 GeneticVariation group BEFREE Our findings strongly suggest that monogenic inheritance of CFH variants can result in basal laminar drusen in young adults, and this can progress to maculopathy and severe vision loss later in life. 18252232 2008