Gene: CRB1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23418
Gene Symbol: CRB1
CRB1 		0.110 CausalMutation disease CLINVAR A clinical and molecular characterisation of CRB1-associated maculopathy. 29391521 2018
Entrez Id: 23418
Gene Symbol: CRB1
CRB1 		0.110 GeneticVariation disease BEFREE We performed a retrospective review of electronic patient records to identify patients with macular dystrophy due to bi-allelic variants in CRB1. 29391521 2018
Entrez Id: 23418
Gene Symbol: CRB1
CRB1 		0.110 GeneticVariation disease CLINVAR Gene symbol: CRB1. Disease: Leber congenital amaurosis. Accession #Hd0510. 17297678 2006
Entrez Id: 23418
Gene Symbol: CRB1
CRB1 		0.110 CausalMutation disease CLINVAR Leber congenital amaurosis: comprehensive survey of the genetic heterogeneity, refinement of the clinical definition, and genotype-phenotype correlations as a strategy for molecular diagnosis. 15024725 2004