FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term bradyopsia 1 ID (Ontology) DOID:0070363 (Human Disease)
Definition A braydopsia that has_material_basis_in homozygous or compound heterozygous mutation in the RGS9 gene on chromosome 17q24.
Also Known As "prolonged electroretinal response suppression 1"
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 Genes
 bradyopsia 1       1
 for disease ribbon | bradyopsia 1       1
 model of | bradyopsia 1       1
Spanning Tree (Parents/Children)
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autosomal recessive disease__
retinal disease______________|
                             bradyopsia
                              |__bradyopsia 1  1 rec.
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Synonyms
  • "prolonged electroretinal response suppression 1" EXACT
Secondary IDs
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MIM:608415