Disease: Cockayne Syndrome, Type II ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cockayne Syndrome, Type II
CUI: C0751038
Disease: Cockayne Syndrome, Type II
0.700 GeneticVariation CLINVAR Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome. 19894250 2010
Cockayne Syndrome, Type II
CUI: C0751038
Disease: Cockayne Syndrome, Type II
0.700 GeneticVariation CLINVAR Differential requirement for the ATPase domain of the Cockayne syndrome group B gene in the processing of UV-induced DNA damage and 8-oxoguanine lesions in human cells. 11809892 2002