FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term optic atrophy 10 ID (Ontology) DOID:0111434 (Human Disease)
Definition An optic atrophy characterized by early-onset optic neuropathy and mitochondrial defects that has_material_basis_in homozygous or compound heterozygous mutation in the RTN4IP1 gene on chromosome 6q21.
Also Known As "OPA10" ; "optic atrophy 10 with or without ataxia, mental retardation, and seizures"
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 Genes
 optic atrophy 10       1
 for disease ribbon | optic atrophy 10       1
 model of | optic atrophy 10       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
optic nerve disease             |
 |__optic atrophy_______________|
                                optic atrophy 10  1 rec.
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Is a autosomal dominant disease
optic atrophy
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Synonyms
  • "OPA10" EXACT OMO:0003012
    "optic atrophy 10 with or without ataxia, mental retardation, and seizures" EXACT
Secondary IDs
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MIM:616732