Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7439
Gene Symbol: BEST1
BEST1 		0.520 GermlineCausalMutation disease ORPHANET Variant phenotype of Best vitelliform macular dystrophy associated with compound heterozygous mutations in VMD2. 16754206 2006
Entrez Id: 7439
Gene Symbol: BEST1
BEST1 		0.520 GeneticVariation disease BEFREE Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration. 10854112 2000
Entrez Id: 7439
Gene Symbol: BEST1
BEST1 		0.520 Biomarker disease BEFREE Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease). 9700209 1998
Entrez Id: 7439
Gene Symbol: BEST1
BEST1 		0.520 Biomarker disease CTD_human
Entrez Id: 5961
Gene Symbol: PRPH2
PRPH2 		0.300 Biomarker disease CTD_human
Entrez Id: 3617
Gene Symbol: IMPG1
IMPG1 		0.300 Biomarker disease CTD_human
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		0.300 Biomarker disease CTD_human