Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Retinal Nonattachment, Nonsyndromic Congenital ATOH7 disease C1857299 GeneticVariation 0.52 disgenet
Retinal Nonattachment, Nonsyndromic Congenital ATOH7 disease C1857299 Biomarker 0.52 disgenet
Retinal Nonattachment, Nonsyndromic Congenital ATOH7 disease C1857299 GermlineCausalMutation 0.52 disgenet
Retinal Nonattachment, Nonsyndromic Congenital FZD4 disease C1857299 GeneticVariation 0.31 disgenet
Retinal Nonattachment, Nonsyndromic Congenital FZD4 disease C1857299 GermlineCausalMutation 0.31 disgenet
Retinal Nonattachment, Nonsyndromic Congenital SNORD35B disease C1857299 Biomarker 0.01 disgenet
Retinal Nonattachment, Nonsyndromic Congenital SNORD14E disease C1857299 Biomarker 0.01 disgenet
Retinal Nonattachment, Nonsyndromic Congenital SNORA65 disease C1857299 Biomarker 0.01 disgenet
Retinal Nonattachment, Nonsyndromic Congenital COL2A1 disease C1857299 GeneticVariation 0.01 disgenet
Retinal Nonattachment, Nonsyndromic Congenital NDP disease C1857299 GeneticVariation 0.01 disgenet
Retinal Nonattachment, Nonsyndromic Congenital SNORD15A disease C1857299 Biomarker 0.01 disgenet
Retinal Nonattachment, Nonsyndromic Congenital SNORD14C disease C1857299 Biomarker 0.01 disgenet
Retinal Nonattachment, Nonsyndromic Congenital NEUROD1 disease C1857299 GeneticVariation 0.01 disgenet
Retinal Nonattachment, Nonsyndromic Congenital SNORD14D disease C1857299 Biomarker 0.01 disgenet
Retinal Nonattachment, Nonsyndromic Congenital RNANC disease C1857299 GeneticVariation 0.01 disgenet
Retinal Nonattachment, Nonsyndromic Congenital SNORD14B disease C1857299 Biomarker 0.01 disgenet
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