Gilbert disease

Disease Term Disease ID Gene Symbol Classification References Source
Gilbert Disease (disorder) C0017551 UGT1A1 Causal Pathogenic evidence from ClinVar 7715297, 9627603, 10421657, 11013440, 12139570, 15180166, 15297419, 17496722 ClinVar
UGT1A Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 22213127 -
UGT1A10 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
UGT1A3 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
UGT1A4 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
UGT1A5 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
UGT1A6 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
UGT1A7 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
UGT1A8 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
UGT1A9 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
NON RARE IN EUROPE: Gilbert syndrome 357 UGT1A1 Causal Pathogenic evidence from ClinVar - ClinVar