Disease Term Disease ID Gene Symbol Classification References Source
Optic atrophy, intellectual disability syndrome C3810363 NR2F1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 24462372, 26986877 -
NR2F1-AS1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 26986877 -
Optic atrophy-intellectual disability syndrome 401777 NR2F1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -