Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4041
Gene Symbol: LRP5
LRP5
0.700 Biomarker disease GENOMICS_ENGLAND Novel Homozygous LRP5 Mutations in Mexican Patients with Osteoporosis-Pseudoglioma Syndrome. 29131652 2017
Entrez Id: 4041
Gene Symbol: LRP5
LRP5
0.700 GeneticVariation disease UNIPROT Identification of two novel LRP5 mutations in families with familial exudative vitreoretinopathy. 24715757 2014
Entrez Id: 4041
Gene Symbol: LRP5
LRP5
0.700 GeneticVariation disease UNIPROT Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP. 20340138 2010
Entrez Id: 4041
Gene Symbol: LRP5
LRP5
0.700 GeneticVariation disease UNIPROT Clinical and molecular evaluation of probands and family members with familial exudative vitreoretinopathy. 19324841 2009
Entrez Id: 4041
Gene Symbol: LRP5
LRP5
0.700 GeneticVariation disease UNIPROT Reduced bone mineral density and hyaloid vasculature remnants in a consanguineous recessive FEVR family with a mutation in LRP5. 16929062 2006
Entrez Id: 4041
Gene Symbol: LRP5
LRP5
0.700 GeneticVariation disease UNIPROT Clinical and molecular findings in osteoporosis-pseudoglioma syndrome. 16252235 2005
Entrez Id: 4041
Gene Symbol: LRP5
LRP5
0.700 GeneticVariation disease UNIPROT Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes. 15981244 2005
Entrez Id: 4041
Gene Symbol: LRP5
LRP5
0.700 GeneticVariation disease UNIPROT Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q. 15024691 2004
Entrez Id: 4041
Gene Symbol: LRP5
LRP5
0.700 GeneticVariation disease UNIPROT Autosomal recessive familial exudative vitreoretinopathy is associated with mutations in LRP5. 15346351 2004
Entrez Id: 4041
Gene Symbol: LRP5
LRP5
0.700 Biomarker disease GENOMICS_ENGLAND LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development. 11719191 2001
Entrez Id: 4041
Gene Symbol: LRP5
LRP5
0.700 CausalMutation disease CLINVAR
Entrez Id: 4041
Gene Symbol: LRP5
LRP5
0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 4041
Gene Symbol: LRP5
LRP5
0.700 Biomarker disease CTD_human