Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9227
Gene Symbol: LRAT
LRAT
0.120 GeneticVariation phenotype BEFREE Leber congenital amaurosis, caused by mutations in RPE65 and LRAT, is a severe form of inherited retinal degeneration leading to blindness. 25030840 2014
Entrez Id: 9227
Gene Symbol: LRAT
LRAT
0.120 GeneticVariation phenotype LHGDN Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa. 17438524 2007
Entrez Id: 9227
Gene Symbol: LRAT
LRAT
0.120 Biomarker phenotype HPO