Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 83552
Gene Symbol: MFRP
MFRP
0.020 Biomarker phenotype LHGDN Our data indicate that defects in MFRP could be responsible for syndromic forms of microphthalmos/retinal degeneration and that this gene is necessary for photoreceptor maintenance. 17167404 2006
Entrez Id: 83552
Gene Symbol: MFRP
MFRP
0.020 GeneticVariation phenotype LHGDN Mutation screen of the membrane-type frizzled-related protein (MFRP) gene in patients with inherited retinal degenerations. 16352475 2005