Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4036
Gene Symbol: LRP2
LRP2
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.120 Biomarker BEFREE Postnatal loss of megalin in the RPE induces dramatic and rapid ocular growth and retinal degeneration compatible with the high myopia observed in Donnai-Barrow patients. 30665232

2019
Entrez Id: 4036
Gene Symbol: LRP2
LRP2
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.120 Biomarker BEFREE Megalin-deficiency causes high myopia, retinal pigment epithelium-macromelanosomes and abnormal development of the ciliary body in mice. 24980834

2014